A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5473629



Internal ID251315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:81937968..81947038hg38UCSC Ensembl
chr6:82647685..82656755hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg389071
hg199071
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16983957
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5473629
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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