A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5478523



Internal ID256075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:117232722..117232778hg38UCSC Ensembl
chr7:116872776..116872832hg19UCSC Ensembl
Cytoband7q31.2
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17004260
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5478523
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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