A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv666614



Internal ID15056580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:3563003..3575447hg38UCSC Ensembl
Innerchr16:3613004..3625448hg19UCSC Ensembl
Innerchr16:3553005..3565449hg18UCSC Ensembl
Innerchr16:3553005..3565449hg17UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3812445
hg1912445
hg1812445
hg1712445
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517451
Supporting Variants
Samples
Known GenesNLRC3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv666614
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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