A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5491134



Internal ID268378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:141507495..141508639hg38UCSC Ensembl
chr7:141207295..141208439hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg381145
hg191145
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17004435
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5491134
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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