A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv668450



Internal ID15058416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:70660097..70737376hg38UCSC Ensembl
Innerchr16:70694000..70771279hg19UCSC Ensembl
Innerchr16:69251501..69328780hg18UCSC Ensembl
Innerchr16:69251501..69328780hg17UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3877280
hg1977280
hg1877280
hg1777280
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517391
Supporting Variants
Samples
Known GenesIL34, MTSS1L, VAC14
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv668450
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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