A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039621



Internal ID18782152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30656421..30818328hg38UCSC Ensembl
Innerchr15:30948624..31110531hg19UCSC Ensembl
Innerchr15:28735916..28897823hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38161908
hg19161908
hg18161908
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2533n100
Supporting Variantsnssv3547651
Samples
Known GenesHERC2P10, LOC100288637
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039621
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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