A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3999568



Internal ID19188198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:99025994..99026108hg38UCSC Ensembl
Outerchr13:99678248..99678362hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg38115
hg19115
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1146368
Supporting Variants
SamplesKWB1
Known GenesDOCK9
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3999568
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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