A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4735446



Internal ID20511388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:43808444..43808500hg38UCSC Ensembl
chr7:43848043..43848099hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16287650
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4735446
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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