A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14314949



Internal ID22190395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:39660415..39666954hg38UCSC Ensembl
chr4:39662035..39668574hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg386540
hg196540
Variant TypeCNV duplication
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3208638
Supporting Variants
SamplesHG00731
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14314949
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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