A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17559528



Internal ID21883883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:149108634..149108744hg38UCSC Ensembl
chr7:148805726..148805836hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6014529
Supporting Variants
Samples
Known GenesZNF425
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17559528
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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