A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697841



Internal ID15434493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:21160216..21175893hg38UCSC Ensembl
Innerchr6:21160447..21176124hg19UCSC Ensembl
Innerchr6:21268426..21284103hg18UCSC Ensembl
Innerchr6:21268426..21284103hg17UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3815678
hg1915678
hg1815678
hg1715678
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521200
Supporting Variants
Samples
Known GenesCDKAL1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697841
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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