A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3998765



Internal ID18846472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:38528464..38528744hg38UCSC Ensembl
Outerchr21:39900388..39900668hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1149979
Supporting Variants
SamplesKWB1
Known GenesERG
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3998765
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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