A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696580



Internal ID15086546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:89100686..89197443hg38UCSC Ensembl
Innerchr16:89167094..89263851hg19UCSC Ensembl
Innerchr16:87694595..87791352hg18UCSC Ensembl
Innerchr16:87694595..87791352hg17UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3896758
hg1996758
hg1896758
hg1796758
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519104
Supporting Variants
Samples
Known GenesACSF3, CDH15, LINC00304, LOC400558, SLC22A31
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696580
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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