A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4739339



Internal ID20515312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:41527075..41527156hg38UCSC Ensembl
chr1:41992746..41992827hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16280778
Samples
Known GenesHIVEP3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4739339
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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