A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv682038



Internal ID15072004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:54031284..54044202hg38UCSC Ensembl
Innerchr20:52647823..52660741hg19UCSC Ensembl
Innerchr20:52081230..52094148hg18UCSC Ensembl
Innerchr20:52081230..52094148hg17UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3812919
hg1912919
hg1812919
hg1712919
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517164
Supporting Variants
Samples
Known GenesBCAS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv682038
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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