A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3525241



Internal ID22394617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:83088949..83089016hg38UCSC Ensembl
chr4:84010102..84010169hg19UCSC Ensembl
Cytoband4q21.22
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14315803, nssv14315802
SamplesHG00732, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3525241
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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