A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3003207



Internal ID17296159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:34889395..34889497hg38UCSC Ensembl
Outerchr20:33477198..33477300hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv956232
Supporting Variants
SamplesBILGI_BIOE
Known GenesACSS2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3003207
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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