A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036203



Internal ID19125422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:19998696..20512131hg38UCSC Ensembl
Innerchr15:20203949..20717374hg19UCSC Ensembl
Innerchr15:18463963..18977388hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38513436
hg19513426
hg18513426
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2186n100
Supporting Variantsnssv3534506, nssv3534505, nssv3534504
Samples
Known GenesCHEK2P2, HERC2P3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036203
Frequency
Sample Size11257
Observed Gain2
Observed Loss1
Observed Complex0
Frequencyn/a


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