A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518641



Internal ID15099248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:1645775..1835631hg38UCSC Ensembl
Innerchr16:1695776..1885632hg19UCSC Ensembl
Innerchr16:1635777..1825633hg18UCSC Ensembl
Innerchr16:1635777..1825633hg17UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38189857
hg19189857
hg18189857
hg17189857
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696091
Samples
Known GenesCRAMP1L, EME2, FAHD1, HAGH, HN1L, IGFALS, MAPK8IP3, MEIOB, MIR3177, MRPS34, NME3, NUBP2, SPSB3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518641
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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