A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519443



Internal ID15446736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:11412452..11424918hg38UCSC Ensembl
Innerchr16:11506308..11518774hg19UCSC Ensembl
Innerchr16:11413809..11426275hg18UCSC Ensembl
Innerchr16:11413809..11426275hg17UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3812467
hg1912467
hg1812467
hg1712467
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv676849, nssv656207, nssv672349, nssv657134
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519443
Frequency
Sample Size2026
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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