A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041363



Internal ID19130582
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+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2273n100
Supporting Variantsnssv3537191, nssv3537184, nssv3537181, nssv3537177, nssv3537175, nssv3537187, nssv3537190, nssv3714600, nssv3714602, nssv3537178, nssv3537183, nssv3537193, nssv3714598, nssv3537189, nssv3537172, nssv3714601, nssv3537182, nssv3537169, nssv3537188, nssv3537168, nssv3714599, nssv3537180, nssv3537174, nssv3537192, nssv3537176, nssv3537171, nssv3537170, nssv3537173, nssv3537185, nssv3537179, nssv3537186
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)nsv1041363
Frequency
Sample Size11257
Observed Gain16
Observed Loss15
Observed Complex0
Frequencyn/a


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