A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052901



Internal ID19142120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20011690..20441310hg38UCSC Ensembl
Innerchr15:20216943..20646563hg19UCSC Ensembl
Innerchr15:18476957..18906577hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38429621
hg19429621
hg18429621
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2185n100
Supporting Variantsnssv3536942, nssv3536943, nssv3536941, nssv3715755
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)nsv1052901
Frequency
Sample Size11257
Observed Gain3
Observed Loss1
Observed Complex0
Frequencyn/a


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