A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701836



Internal ID15438488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:86022231..86083815hg38UCSC Ensembl
Innerchr1:86487914..86549498hg19UCSC Ensembl
Innerchr1:86260502..86322086hg18UCSC Ensembl
Innerchr1:86199935..86261519hg17UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg3861585
hg1961585
hg1861585
hg1761585
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525678
Supporting Variants
Samples
Known GenesCOL24A1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701836
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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