A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17447874



Internal ID22505744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:535729..536042hg38UCSC Ensembl
chr7:575366..575679hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5922554
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17447874
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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