A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv665204



Internal ID15055170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:3549655..3583656hg38UCSC Ensembl
Innerchr16:3599655..3633657hg19UCSC Ensembl
Innerchr16:3539656..3573658hg18UCSC Ensembl
Innerchr16:3539656..3573658hg17UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3834002
hg1934003
hg1834003
hg1734003
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)nssv665204
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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