A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3964481



Internal ID19230035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:35249171..35250146hg38UCSC Ensembl
Outerchr22:35645164..35646139hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38976
hg19976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1121247
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3964481
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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