A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5462845



Internal ID240766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:36888745..36888922hg38UCSC Ensembl
chr6:36856521..36856698hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg38178
hg19178
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16982090
Samples
Known GenesC6orf89
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5462845
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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