A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053984



Internal ID19143203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:94235844..94281603hg38UCSC Ensembl
Innerchr15:94779073..94824832hg19UCSC Ensembl
Innerchr15:92580077..92625836hg18UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3845760
hg1945760
hg1845760
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2665n100
Supporting Variantsnssv3555269, nssv3555270
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)nsv1053984
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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