A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3961124



Internal ID18858081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:3421134..3421195hg38UCSC Ensembl
Outerchr18:3421132..3421193hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1110716
Supporting Variants
SamplesKWS1
Known GenesTGIF1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3961124
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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