A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv842496



Internal ID15789766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:48097727..48128547hg38UCSC Ensembl
Innerchr15:48389924..48420744hg19UCSC Ensembl
Innerchr15:46177216..46208036hg18UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg3830821
hg1930821
hg1830821
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv569337
Supporting Variants
Samples
Known GenesSLC24A5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv842496
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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