A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047340



Internal ID19136559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20380825..20512131hg38UCSC Ensembl
Innerchr15:20586078..20717374hg19UCSC Ensembl
Innerchr15:18846092..18977388hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38131307
hg19131297
hg18131297
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2265n100
Supporting Variantsnssv3714730, nssv3714729
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)nsv1047340
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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