A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4750009



Internal ID20526044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:129977158..129977317hg38UCSC Ensembl
chr7:129616998..129617157hg19UCSC Ensembl
Cytoband7q32.2
Allele length
AssemblyAllele length
hg38160
hg19160
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16261484
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4750009
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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