A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528954



Internal ID15109561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:142445175..142500700hg38UCSC Ensembl
Innerchr3:142164017..142219542hg19UCSC Ensembl
Innerchr3:143646707..143702232hg18UCSC Ensembl
Innerchr3:143646715..143702240hg17UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg3855526
hg1955526
hg1855526
hg1755526
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705650
Samples
Known GenesATR, XRN1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528954
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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