A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009938



Internal ID19099157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:19786025..19847374hg38UCSC Ensembl
Innerchr4:19787648..19848997hg19UCSC Ensembl
Innerchr4:19396746..19458095hg18UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg3861350
hg1961350
hg1861350
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3619879
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)nsv1009938
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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