A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3950742



Internal ID21370811
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 Variantsnssv15198838
SamplesHG002
Known GenesUBE2W
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3950742
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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