A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6398071



Internal ID21055624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:69135006..69141526hg38UCSC Ensembl
chr5:68430833..68437353hg19UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg386521
hg196521
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18133318
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6398071
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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