A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522507



Internal ID15449800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:3846662..3849827hg38UCSC Ensembl
Innerchr20:3827309..3830474hg19UCSC Ensembl
Innerchr20:3775309..3778474hg18UCSC Ensembl
Innerchr20:3775309..3778474hg17UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg383166
hg193166
hg183166
hg173166
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705875
Samples
Known GenesMAVS
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522507
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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