A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1122071



Internal ID18903395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:134575058..134575758hg38UCSC Ensembl
Outerchr3:134293900..134294600hg19UCSC Ensembl
Cytoband3q22.2
Allele length
AssemblyAllele length
hg38701
hg19701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2605n106
Supporting Variantsnssv3969507
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1122071
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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