A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039022



Internal ID19128241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20380723..20512131hg38UCSC Ensembl
Innerchr15:20585976..20717374hg19UCSC Ensembl
Innerchr15:18845990..18977388hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38131409
hg19131399
hg18131399
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2243n100
Supporting Variantsnssv3537194, nssv3537198, nssv3537199, nssv3537200, nssv3537205, nssv3714604, nssv3714609, nssv3714606, nssv3714607, nssv3714605, nssv3537203, nssv3537204, nssv3537202, nssv3537197, nssv3714608, nssv3537201, nssv3537196, nssv3537195, nssv3714603
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)nsv1039022
Frequency
Sample Size11257
Observed Gain6
Observed Loss13
Observed Complex0
Frequencyn/a


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