A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524942



Internal ID15452235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:25938859..26009513hg38UCSC Ensembl
Innerchr16:25950180..26020834hg19UCSC Ensembl
Innerchr16:25857681..25928335hg18UCSC Ensembl
Innerchr16:25857681..25928335hg17UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3870655
hg1970655
hg1870655
hg1770655
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv164n21
Supporting Variantsnssv700959
Samples
Known GenesHS3ST4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524942
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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