A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17439412



Internal ID22497282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:2346486..2347219hg38UCSC Ensembl
chr7:2386121..2386854hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38734
hg19734
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5911950
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17439412
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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