A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv842497



Internal ID15789767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:48104611..48160602hg38UCSC Ensembl
Innerchr15:48396808..48452799hg19UCSC Ensembl
Innerchr15:46184100..46240091hg18UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg3855992
hg1955992
hg1855992
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv569338
Supporting Variants
Samples
Known GenesMYEF2, SLC24A5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv842497
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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