A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv653888



Internal ID15043854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:151796802..151828253hg38UCSC Ensembl
Innerchr3:151514590..151546041hg19UCSC Ensembl
Innerchr3:152997280..153028731hg18UCSC Ensembl
Innerchr3:152997288..153028739hg17UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3831452
hg1931452
hg1831452
hg1731452
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517155
Supporting Variants
Samples
Known GenesAADAC, MIR548H2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv653888
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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