A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17442442



Internal ID22500312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:142313665..142797124hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38483460
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5907712
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17442442
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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