A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3986546



Internal ID18878650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:177158241..177158320hg38UCSC Ensembl
Outerchr5:176585242..176585321hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1131929
Supporting Variants
SamplesKWS1
Known GenesNSD1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3986546
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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