A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3980601



Internal ID19206451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:38382645..38387482hg38UCSC Ensembl
Outerchr22:38778650..38783487hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg384838
hg194838
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1143410
Supporting Variants
SamplesKWS1
Known GenesLOC400927
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3980601
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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