A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3974888



Internal ID19242543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:13399840..13399920hg38UCSC Ensembl
Outerchr5:13399952..13400032hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1136970
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3974888
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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