A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6002034



Internal ID21911377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:88668939..88669447hg38UCSC Ensembl
chr10:90428696..90429204hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg38509
hg19509
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17588500
Samples
Known GenesLIPF
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6002034
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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