A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3981739



Internal ID19220163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:39557395..39558195hg38UCSC Ensembl
Outerchr22:39953400..39954200hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg38801
hg19801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1118952
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3981739
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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