A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17566544



Internal ID21758587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:146049731..146058519hg38UCSC Ensembl
chr7:145746824..145755612hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg388789
hg198789
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6007990
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17566544
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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