A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3967110



Internal ID19243148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:45349418..45350362hg38UCSC Ensembl
Outerchr22:45745299..45746243hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg38945
hg19945
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1130790
Supporting Variants
SamplesKWS2
Known GenesSMC1B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3967110
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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