A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061003



Internal ID19150222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:53425499..53503054hg38UCSC Ensembl
Innerchr19:53928752..54006308hg19UCSC Ensembl
Innerchr19:58620564..58698120hg18UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg3877556
hg1977557
hg1877557
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3649n100
Supporting Variantsnssv3573251, nssv3726528, nssv3573250
Samples
Known GenesTPM3P9, ZNF761, ZNF813
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1061003
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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