A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3961188



Internal ID19220193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:173399522..173399574hg38UCSC Ensembl
Outerchr4:174320673..174320725hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1110779
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3961188
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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