A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3974624



Internal ID18888509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:115654880..115654953hg38UCSC Ensembl
Outerchr5:114990577..114990650hg19UCSC Ensembl
Cytoband5q22.3
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1123975
Supporting Variants
SamplesKWS2
Known GenesLOC102467217
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3974624
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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