A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv597037



Internal ID16384446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:8702973..8746994hg38UCSC Ensembl
Innerchr5:8703085..8747106hg19UCSC Ensembl
Innerchr5:8756085..8800106hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3844022
hg1944022
hg1844022
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9569n54
Supporting Variantsnssv1023969, nssv1023980, nssv1023930, nssv1023997, nssv1023998, nssv1023994, nssv1023932, nssv1023939, nssv1023950, nssv1023955, nssv1023973, nssv1023979, nssv1023957, nssv1023990, nssv1023946, nssv1023987, nssv1023947, nssv1023983, nssv1023943, nssv1023962, nssv1023958, nssv1023965, nssv1023938, nssv1024000, nssv1023948, nssv1023945, nssv1023988, nssv1023974, nssv1023936, nssv1024004, nssv1023953, nssv1023976, nssv1023977, nssv1023993, nssv1024003, nssv1023941, nssv1023937, nssv1023963, nssv1023981, nssv1023975, nssv1023985, nssv1023971, nssv1023933, nssv1023956, nssv1024002, nssv1023968, nssv1023992, nssv1023961, nssv1023960, nssv1023949, nssv1023934, nssv1023931, nssv1023970, nssv1023966, nssv1023984, nssv1023951, nssv1023982, nssv1023967, nssv1023964, nssv1023972, nssv1023991, nssv1023952, nssv1023935, nssv1023942, nssv1023989, nssv1023959, nssv1023954, nssv1023944, nssv1023999, nssv1023996, nssv1023986, nssv1023940, nssv1024001, nssv1023995, nssv1023978
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv597037
Frequency
Sample Size17421
Observed Gain0
Observed Loss75
Observed Complex0
Frequencyn/a


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