A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705954



Internal ID15095920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:82955372..83011060hg38UCSC Ensembl
Innerchr16:82988977..83044665hg19UCSC Ensembl
Innerchr16:81546478..81602166hg18UCSC Ensembl
Innerchr16:81546478..81602166hg17UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3855689
hg1955689
hg1855689
hg1755689
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522570
Supporting Variants
Samples
Known GenesCDH13
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705954
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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