A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17439991



Internal ID22497861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:4567790..4633574hg38UCSC Ensembl
chr7:4607421..4673205hg19UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg3865785
hg1965785
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5908898
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17439991
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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