A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3529621



Internal ID22399013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:73875526..73875623hg38UCSC Ensembl
chr8:74787761..74787858hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14343189, nssv14343187, nssv14343188
SamplesNA19238, HG00731, HG00733
Known GenesUBE2W
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3529621
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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