A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3965502



Internal ID19239252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:113336623..113336818hg38UCSC Ensembl
Outerchr13:113990938..113991133hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38196
hg19196
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1121501
Supporting Variants
SamplesKWS2
Known GenesGRTP1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3965502
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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