A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3978174



Internal ID18866976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:108256721..108796820hg38UCSC Ensembl
Outerchr13:108909069..109449168hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg38540100
hg19540100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1139838
Supporting Variants
SamplesKWS1
Known GenesMYO16, TNFSF13B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3978174
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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