A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526299



Internal ID15106906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:85651514..85667980hg38UCSC Ensembl
Innerchr16:85685120..85701586hg19UCSC Ensembl
Innerchr16:84242621..84259087hg18UCSC Ensembl
Innerchr16:84242621..84259087hg17UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3816467
hg1916467
hg1816467
hg1716467
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702580
Samples
Known GenesGSE1, MIR7851
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526299
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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