A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705836



Internal ID15095802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:151743597..151864407hg38UCSC Ensembl
Innerchr3:151461385..151582195hg19UCSC Ensembl
Innerchr3:152944075..153064885hg18UCSC Ensembl
Innerchr3:152944083..153064893hg17UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg38120811
hg19120811
hg18120811
hg17120811
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522472
Supporting Variants
Samples
Known GenesAADAC, AADACL2, LOC201651, MIR548H2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705836
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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