A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv666649



Internal ID15056615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:238127212..238152125hg38UCSC Ensembl
Innerchr2:239035853..239060766hg19UCSC Ensembl
Innerchr2:238700592..238725505hg18UCSC Ensembl
Innerchr2:238817853..238842766hg17UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg3824914
hg1924914
hg1824914
hg1724914
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517412
Supporting Variants
Samples
Known GenesESPNL, KLHL30
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv666649
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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