A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4000107



Internal ID18843376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:33344782..33344837hg38UCSC Ensembl
Outerchr22:33740768..33740823hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1147335
Supporting Variants
SamplesKWB1
Known GenesLARGE
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv4000107
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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