A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694271



Internal ID15084237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:75529848..75538114hg38UCSC Ensembl
Innerchr16:75563746..75572012hg19UCSC Ensembl
Innerchr16:74121247..74129513hg18UCSC Ensembl
Innerchr16:74121247..74129513hg17UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg388267
hg198267
hg188267
hg178267
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516675
Supporting Variants
Samples
Known GenesCHST5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694271
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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