A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3000006



Internal ID16946272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:58996546..59007245hg38UCSC Ensembl
Outerchr20:57571601..57582300hg19UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg3810700
hg1910700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv955144
Supporting Variants
SamplesBILGI_BIOE
Known GenesCTSZ
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3000006
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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