A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699666



Internal ID15436318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:37378728..37453742hg38UCSC Ensembl
Innerchr20:36007131..36082144hg19UCSC Ensembl
Innerchr20:35440545..35515558hg18UCSC Ensembl
Innerchr20:35440545..35515558hg17UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3875015
hg1975014
hg1875014
hg1775014
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523834
Supporting Variants
Samples
Known GenesSRC
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699666
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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