A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3963323



Internal ID18888285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:150307007..150307111hg38UCSC Ensembl
Outerchr5:149686570..149686674hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1120875
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3963323
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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