A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1136673



Internal ID18920204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:35611786..35611885hg38UCSC Ensembl
Outerchr22:36007833..36007932hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3973061
SamplesKWS2
Known GenesMB
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1136673
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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