A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3981581



Internal ID18877343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:37905993..37906693hg38UCSC Ensembl
Outerchr22:38302000..38302700hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg38701
hg19701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1144971
Supporting Variants
SamplesKWS1
Known GenesMICALL1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3981581
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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