A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16993972



Internal ID63430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:26230260..26230450hg38UCSC Ensembl
chr7:26269880..26270070hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg38191
hg19191
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5482994
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16993972
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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