A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4739331



Internal ID20515304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:111841805..111841940hg38UCSC Ensembl
chr10:113601563..113601698hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg38136
hg19136
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16280401
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4739331
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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