A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17559312



Internal ID21883667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:40882794..40884782hg38UCSC Ensembl
chr7:40922393..40924381hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg381989
hg191989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6009464
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17559312
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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