A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050148



Internal ID19139367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20396289..20441310hg38UCSC Ensembl
Innerchr15:20601542..20646563hg19UCSC Ensembl
Innerchr15:18861556..18906577hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3845022
hg1945022
hg1845022
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2277n100
Supporting Variantsnssv3539656, nssv3539657
Samples
Known GenesHERC2P3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1050148
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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