A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3969777



Internal ID19220400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:90564604..90564925hg38UCSC Ensembl
Outerchr5:89860421..89860742hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1130512
Supporting Variants
SamplesKWS1
Known GenesGPR98
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3969777
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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