A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv670652



Internal ID15060618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:127039538..127101865hg38UCSC Ensembl
Innerchr2:127797114..127859441hg19UCSC Ensembl
Innerchr2:127513584..127575911hg18UCSC Ensembl
Innerchr2:127513344..127575671hg17UCSC Ensembl
Cytoband2q14.3
Allele length
AssemblyAllele length
hg3862328
hg1962328
hg1862328
hg1762328
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516759
Supporting Variants
Samples
Known GenesBIN1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv670652
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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