A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704040



Internal ID15094006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:86495174..86518176hg38UCSC Ensembl
Innerchr16:86528780..86551782hg19UCSC Ensembl
Innerchr16:85086281..85109283hg18UCSC Ensembl
Innerchr16:85086281..85109283hg17UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3823003
hg1923003
hg1823003
hg1723003
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527579
Supporting Variants
Samples
Known GenesFENDRR, FOXF1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704040
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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