A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1140174



Internal ID19267783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:197032584..197034764hg38UCSC Ensembl
Outerchr3:196759455..196761635hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg382181
hg192181
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2690n106
Supporting Variantsnssv3978886
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1140174
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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