A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv597036



Internal ID16384445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:8702973..8744445hg38UCSC Ensembl
Innerchr5:8703085..8744557hg19UCSC Ensembl
Innerchr5:8756085..8797557hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3841473
hg1941473
hg1841473
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9569n54
Supporting Variantsnssv1023926, nssv1023929, nssv1023927, nssv1023924, nssv1023923, nssv1023928, nssv1023925
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv597036
Frequency
Sample Size17421
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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