A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv843581



Internal ID16137537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:59437058..59438731hg38UCSC Ensembl
Innerchr15:59729257..59730930hg19UCSC Ensembl
Innerchr15:57516549..57518222hg18UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg381674
hg191674
hg181674
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv569604
Supporting Variants
Samples
Known GenesFAM81A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv843581
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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