A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048639



Internal ID19137858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20305889..20512131hg38UCSC Ensembl
Innerchr15:20511142..20717374hg19UCSC Ensembl
Innerchr15:18771156..18977388hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38206243
hg19206233
hg18206233
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2235n100
Supporting Variantsnssv3536098
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)nsv1048639
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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