A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv692915



Internal ID15429567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:364930..382751hg38UCSC Ensembl
Innerchr16:414930..432751hg19UCSC Ensembl
Innerchr16:354931..372752hg18UCSC Ensembl
Innerchr16:354931..372752hg17UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3817822
hg1917822
hg1817822
hg1717822
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517471
Supporting Variants
Samples
Known GenesLOC100134368, MRPL28, TMEM8A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv692915
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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