A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3981693



Internal ID18872581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:159971893..159972693hg38UCSC Ensembl
Outerchr5:159398900..159399700hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg38801
hg19801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1145074
Supporting Variants
SamplesKWS1
Known GenesADRA1B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3981693
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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