A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4731491



Internal ID20507412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:90290751..90290812hg38UCSC Ensembl
chr7:89920065..89920126hg19UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16272429
Samples
Known GenesC7orf63
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4731491
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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