A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv669454



Internal ID15406106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:44886246..44902938hg38UCSC Ensembl
Innerchr21:46306161..46322853hg19UCSC Ensembl
Innerchr21:45130589..45147281hg18UCSC Ensembl
Innerchr21:45130589..45147281hg17UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3816693
hg1916693
hg1816693
hg1716693
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516593
Supporting Variants
Samples
Known GenesITGB2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv669454
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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