A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv651803



Internal ID15041769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:109262024..109275908hg38UCSC Ensembl
Innerchr1:109804646..109818530hg19UCSC Ensembl
Innerchr1:109606169..109620053hg18UCSC Ensembl
Innerchr1:109516688..109530572hg17UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3813885
hg1913885
hg1813885
hg1713885
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517354
Supporting Variants
Samples
Known GenesCELSR2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv651803
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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