A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6407853



Internal ID21065406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:135370374..135371109hg38UCSC Ensembl
chr5:134706064..134706799hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg38736
hg19736
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18127274
Samples
Known GenesH2AFY
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6407853
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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