A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv665872



Internal ID15055838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:95485211..96006253hg38UCSC Ensembl
Innerchr2:96150959..96672001hg19UCSC Ensembl
Innerchr2:95514686..96035728hg18UCSC Ensembl
Innerchr2:95572833..96093875hg17UCSC Ensembl
Cytoband2q11.1
Allele length
AssemblyAllele length
hg38521043
hg19521043
hg18521043
hg17521043
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516044
Supporting Variants
Samples
Known GenesLINC00342, TRIM43
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv665872
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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