A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041399



Internal ID19130618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20235273..20512131hg38UCSC Ensembl
Innerchr15:20440526..20717374hg19UCSC Ensembl
Innerchr15:18700540..18977388hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38276859
hg19276849
hg18276849
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2221n100
Supporting Variantsnssv3713574, nssv3539460, nssv3539461
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)nsv1041399
Frequency
Sample Size11257
Observed Gain2
Observed Loss1
Observed Complex0
Frequencyn/a


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