A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516692



Internal ID15443985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:13835497..13868202hg38UCSC Ensembl
Innerchr7:13875122..13907827hg19UCSC Ensembl
Innerchr7:13841647..13874352hg18UCSC Ensembl
Innerchr7:13648362..13681067hg17UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg3832706
hg1932706
hg1832706
hg1732706
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv661355, nssv670193
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516692
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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