A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv706038



Internal ID15096004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:19898447..19909300hg38UCSC Ensembl
Innerchr2:20098208..20109061hg19UCSC Ensembl
Innerchr2:19961689..19972542hg18UCSC Ensembl
Innerchr2:20019836..20030689hg17UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg3810854
hg1910854
hg1810854
hg1710854
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522640
Supporting Variants
Samples
Known GenesTTC32
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv706038
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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