A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019250



Internal ID19108468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:133769093..133792042hg38UCSC Ensembl
Innerchr5:133104784..133127733hg19UCSC Ensembl
Innerchr5:133132683..133155632hg18UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg3822950
hg1922950
hg1822950
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5809n100
Supporting Variantsnssv3648119
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1019250
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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