A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5471049



Internal ID248794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:39362873..39363575hg38UCSC Ensembl
chr6:39330649..39331351hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg38703
hg19703
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16981574
Samples
Known GenesKIF6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5471049
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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