A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6008658



Internal ID21918001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:83390581..83455981hg38UCSC Ensembl
chr10:85150337..85215737hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3865401
hg1965401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17588787
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6008658
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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