A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3967299



Internal ID18881876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:41473673..41475073hg38UCSC Ensembl
Outerchr21:42845600..42847000hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg381401
hg191401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1112801
Supporting Variants
SamplesKWS2
Known GenesTMPRSS2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3967299
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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