A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1139098



Internal ID19252376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:16538103..16538153hg38UCSC Ensembl
Outerchr3:16579610..16579660hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3991722, nssv3956969
SamplesKWS2, KWS1
Known GenesLINC00690
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1139098
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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