A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5491371



Internal ID268611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:149438158..149438233hg38UCSC Ensembl
chr7:149135249..149135324hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17004822
Samples
Known GenesZNF777
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5491371
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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