A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17573059



Internal ID21765102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:43714640..43720006hg38UCSC Ensembl
chr7:43754239..43759605hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg385367
hg195367
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6009835
Supporting Variants
Samples
Known GenesCOA1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17573059
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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