A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17577429



Internal ID21769472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:43665012..43665082hg38UCSC Ensembl
chr7:43704611..43704681hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6013651
Supporting Variants
Samples
Known GenesCOA1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17577429
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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