A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3971830



Internal ID19241874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:98353193..98353250hg38UCSC Ensembl
Outerchr13:99005447..99005504hg19UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1134344
Supporting Variants
SamplesKWS2
Known GenesFARP1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3971830
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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