A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589383



Internal ID16376792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:2454047..2454664hg38UCSC Ensembl
Innerchr3:2495731..2496348hg19UCSC Ensembl
Innerchr3:2470731..2471348hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38618
hg19618
hg18618
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8168n54
Supporting Variantsnssv957958, nssv957933, nssv957925, nssv957963, nssv957966, nssv957928, nssv957947, nssv957944, nssv957921, nssv957940, nssv957953, nssv957941, nssv957957, nssv957952, nssv957949, nssv957930, nssv957922, nssv957962, nssv957935, nssv957948, nssv957951, nssv957954, nssv957926, nssv957936, nssv957939, nssv957973, nssv957946, nssv957932, nssv957956, nssv957923, nssv957938, nssv957924, nssv957961, nssv957960, nssv957964, nssv957970, nssv957972, nssv957950, nssv957965, nssv957975, nssv957976, nssv957942, nssv957945, nssv957969, nssv957971, nssv957927, nssv957943, nssv957955, nssv957974, nssv957967, nssv957931, nssv957937, nssv957934, nssv957929, nssv957959, nssv957968
Samples
Known GenesCNTN4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589383
Frequency
Sample Size17421
Observed Gain0
Observed Loss56
Observed Complex0
Frequencyn/a


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