A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703490



Internal ID15093456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:3575447..3577357hg38UCSC Ensembl
Innerchr16:3625448..3627358hg19UCSC Ensembl
Innerchr16:3565449..3567359hg18UCSC Ensembl
Innerchr16:3565449..3567359hg17UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg381911
hg191911
hg181911
hg171911
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)nssv703490
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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