A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3956873



Internal ID19225571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:92198427..92199866hg38UCSC Ensembl
Outerchr5:91494244..91495683hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg381440
hg191440
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1117566
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3956873
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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