A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4734629



Internal ID20510567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:73446621..73446684hg38UCSC Ensembl
chr4:74312338..74312401hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16271820
Samples
Known GenesAFP
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4734629
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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