A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528371



Internal ID15455664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:37378728..37447464hg38UCSC Ensembl
Innerchr20:36007131..36075866hg19UCSC Ensembl
Innerchr20:35440545..35509280hg18UCSC Ensembl
Innerchr20:35440545..35509280hg17UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3868737
hg1968736
hg1868736
hg1768736
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704958
Samples
Known GenesSRC
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528371
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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