A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv976835



Internal ID15924105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:151796802..151833340hg38UCSC Ensembl
Innerchr3:151514590..151551128hg19UCSC Ensembl
Innerchr3:152997280..153033818hg18UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3836539
hg1936539
hg1836539
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv592060
Supporting Variants
Samples
Known GenesAADAC, MIR548H2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv976835
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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