A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3995720



Internal ID19189058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:35249156..35250143hg38UCSC Ensembl
Outerchr22:35645149..35646136hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38988
hg19988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1146565
Supporting Variants
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3995720
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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