A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6397267



Internal ID21054820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:67041726..67042273hg38UCSC Ensembl
chr5:66337554..66338101hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg38548
hg19548
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18132588
Samples
Known GenesMAST4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6397267
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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