A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3000021



Internal ID17292973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:64017648..64160147hg38UCSC Ensembl
Outerchr20:62649001..62791500hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38142500
hg19142500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv953310
Supporting Variants
SamplesBILGI_BIOE
Known GenesC20orf201, LINC00176, MIR6813, NPBWR2, OPRL1, PRPF6, RGS19, SOX18, TCEA2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3000021
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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