A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6015649



Internal ID21924992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:91055626..91055947hg38UCSC Ensembl
chr10:92815383..92815704hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17585805
Samples
Known GenesLINC00502
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6015649
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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