A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702355



Internal ID15439007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:142010949..142126679hg38UCSC Ensembl
Innerchr2:142768518..142884248hg19UCSC Ensembl
Innerchr2:142484988..142600718hg18UCSC Ensembl
Innerchr2:142602250..142717980hg17UCSC Ensembl
Cytoband2q22.2
Allele length
AssemblyAllele length
hg38115731
hg19115731
hg18115731
hg17115731
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526107
Supporting Variants
Samples
Known GenesLRP1B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702355
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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