A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3997969



Internal ID19193273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:34889412..34889500hg38UCSC Ensembl
Outerchr20:33477215..33477303hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1152938
Supporting Variants
SamplesKWB1
Known GenesACSS2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3997969
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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