A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4739827



Internal ID20515803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:78687558..78687622hg38UCSC Ensembl
chr8:79599793..79599857hg19UCSC Ensembl
Cytoband8q21.12
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16291297
Samples
Known GenesZC2HC1A
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4739827
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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