A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3209597



Internal ID22357648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:180567348..180567403hg38UCSC Ensembl
chr4:181488501..181488556hg19UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6985n152
Supporting Variantsnssv14318830, nssv14318829
SamplesHG00731, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3209597
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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