A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698345



Internal ID15088311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:33319157..34037875hg38UCSC Ensembl
Innerchr5:33319263..34037980hg19UCSC Ensembl
Innerchr5:33355020..34073737hg18UCSC Ensembl
Innerchr5:33355020..34073737hg17UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg38718719
hg19718718
hg18718718
hg17718718
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522715
Supporting Variants
Samples
Known GenesADAMTS12, AMACR, C1QTNF3, C1QTNF3-AMACR, RXFP3, SLC45A2, TARS
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698345
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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