A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv686388



Internal ID15423040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:9145396..9150195hg38UCSC Ensembl
Innerchr2:9285525..9290324hg19UCSC Ensembl
Innerchr2:9202976..9207775hg18UCSC Ensembl
Innerchr2:9236123..9240922hg17UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg384800
hg194800
hg184800
hg174800
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517184
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv686388
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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