A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4735539



Internal ID20511482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:105533810..105533923hg38UCSC Ensembl
chr8:106546038..106546151hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg38114
hg19114
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16272046
Samples
Known GenesZFPM2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4735539
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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