A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038247



Internal ID19127466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20380723..20422227hg38UCSC Ensembl
Innerchr15:20585976..20627480hg19UCSC Ensembl
Innerchr15:18845990..18887494hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3841505
hg1941505
hg1841505
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2272n100
Supporting Variantsnssv3714594, nssv3714593, nssv3537158, nssv3537147, nssv3537166, nssv3537146, nssv3714595, nssv3537155, nssv3537150, nssv3537154, nssv3537162, nssv3714597, nssv3537164, nssv3537163, nssv3537165, nssv3537148, nssv3537153, nssv3537167, nssv3537151, nssv3537157, nssv3714592, nssv3537161, nssv3714596, nssv3537160, nssv3537149, nssv3537159, nssv3537152, nssv3537156
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)nsv1038247
Frequency
Sample Size11257
Observed Gain16
Observed Loss12
Observed Complex0
Frequencyn/a


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