A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv684299



Internal ID15074265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:85591521..85651514hg38UCSC Ensembl
Innerchr16:85625127..85685120hg19UCSC Ensembl
Innerchr16:84182628..84242621hg18UCSC Ensembl
Innerchr16:84182628..84242621hg17UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3859994
hg1959994
hg1859994
hg1759994
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515746
Supporting Variants
Samples
Known GenesGSE1, MIR7851
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv684299
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer