A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041894



Internal ID19131113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20060713..20441310hg38UCSC Ensembl
Innerchr15:20265966..20646563hg19UCSC Ensembl
Innerchr15:18525980..18906577hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38380598
hg19380598
hg18380598
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2199n100
Supporting Variantsnssv3538597, nssv3538598
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)nsv1041894
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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