A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3999861



Internal ID18844842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:35776297..35780298hg38UCSC Ensembl
Outerchr19:36267199..36271200hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg384002
hg194002
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1152678
Supporting Variants
SamplesKWB1
Known GenesARHGAP33
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3999861
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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