A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv677941



Internal ID15067907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:1757779..1791032hg38UCSC Ensembl
Innerchr16:1807780..1841033hg19UCSC Ensembl
Innerchr16:1747781..1781034hg18UCSC Ensembl
Innerchr16:1747781..1781034hg17UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3833254
hg1933254
hg1833254
hg1733254
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517196
Supporting Variants
Samples
Known GenesEME2, IGFALS, MAPK8IP3, MRPS34, NME3, NUBP2, SPSB3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv677941
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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