A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3965134



Internal ID19209206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:29148405..29148777hg38UCSC Ensembl
Outerchr13:29722542..29722914hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg38373
hg19373
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1130322
Supporting Variants
SamplesKWS1
Known GenesMTUS2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3965134
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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