A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5460174



Internal ID238168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:13623487..13623550hg38UCSC Ensembl
chr6:13623719..13623782hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16979025
Samples
Known GenesRANBP9
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5460174
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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