A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3208097



Internal ID22356392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:37584952..37585546hg38UCSC Ensembl
chr4:37586574..37587168hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38595
hg19595
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14314878
SamplesHG00732
Known GenesC4orf19
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3208097
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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