A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5461983



Internal ID239922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:33716484..33722382hg38UCSC Ensembl
chr6:33684261..33690159hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg385899
hg195899
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16983548
Samples
Known GenesIP6K3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5461983
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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