A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705135



Internal ID15441787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:62319414..62322665hg38UCSC Ensembl
Innerchr20:60894470..60897721hg19UCSC Ensembl
Innerchr20:60327865..60331116hg18UCSC Ensembl
Innerchr20:60327865..60331116hg17UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg383252
hg193252
hg183252
hg173252
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520024
Supporting Variants
Samples
Known GenesLAMA5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705135
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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