A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5473856



Internal ID251537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:1018714..1019075hg38UCSC Ensembl
chr6:1018949..1019310hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38362
hg19362
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16979866
Samples
Known GenesLOC285768
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5473856
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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