A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17434687



Internal ID22492557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:470289..471310hg38UCSC Ensembl
chr7:509926..510947hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg381022
hg191022
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5909078
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17434687
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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