A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv690444



Internal ID15080410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:75505987..75538025hg38UCSC Ensembl
Innerchr16:75539885..75571923hg19UCSC Ensembl
Innerchr16:74097386..74129424hg18UCSC Ensembl
Innerchr16:74097386..74129424hg17UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3832039
hg1932039
hg1832039
hg1732039
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)nssv690444
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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