A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17573971



Internal ID21766014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:24545837..24546251hg38UCSC Ensembl
chr7:24585456..24585870hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38415
hg19415
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6006930
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17573971
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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