A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5455937



Internal ID234006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:75445722..75451657hg38UCSC Ensembl
chr6:76155438..76161373hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg385936
hg195936
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16985625
Samples
Known GenesFILIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5455937
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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