A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv655260



Internal ID15045226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:3563003..3611814hg38UCSC Ensembl
Innerchr16:3613004..3661815hg19UCSC Ensembl
Innerchr16:3553005..3601816hg18UCSC Ensembl
Innerchr16:3553005..3601816hg17UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3848812
hg1948812
hg1848812
hg1748812
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)nssv655260
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer