A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv679896



Internal ID15069862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:3549655..3589138hg38UCSC Ensembl
Innerchr16:3599655..3639139hg19UCSC Ensembl
Innerchr16:3539656..3579140hg18UCSC Ensembl
Innerchr16:3539656..3579140hg17UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3839484
hg1939485
hg1839485
hg1739485
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)nssv679896
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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