A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527240



Internal ID15107847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:85709458..85761666hg38UCSC Ensembl
Innerchr16:85743064..85795272hg19UCSC Ensembl
Innerchr16:84300565..84352773hg18UCSC Ensembl
Innerchr16:84300565..84352773hg17UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3852209
hg1952209
hg1852209
hg1752209
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703642
Samples
Known GenesC16orf74, MIR1910, MIR7851
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527240
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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