A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16272429



Internal ID20481647
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 StatusS
Merged Variantsnsv4731491
Supporting Variants
Samples
Known GenesC7orf63
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16272429
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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