A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3537186



Internal ID18835467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20380723..20441310hg38UCSC Ensembl
Innerchr15:20585976..20646563hg19UCSC Ensembl
Innerchr15:18845990..18906577hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3860588
hg1960588
hg1860588
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1041363
Supporting Variants
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)nssv3537186
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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