A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5488361



Internal ID265674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:42493713..42499419hg38UCSC Ensembl
chr7:42533312..42539018hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg385707
hg195707
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16996270
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5488361
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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