A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3981799



Internal ID19217472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:68625682..68680082hg38UCSC Ensembl
Outerchr4:69491400..69545800hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg3854401
hg1954401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1119005
Supporting Variants
SamplesKWS1
Known GenesUGT2B15
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3981799
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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