A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv691500



Internal ID15081466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:3549655..3611814hg38UCSC Ensembl
Innerchr16:3599655..3661815hg19UCSC Ensembl
Innerchr16:3539656..3601816hg18UCSC Ensembl
Innerchr16:3539656..3601816hg17UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3862160
hg1962161
hg1862161
hg1762161
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517451
Supporting Variants
Samples
Known GenesNLRC3, SLX4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv691500
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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