A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6407801



Internal ID21065354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:105293113..106123235hg38UCSC Ensembl
chr5:104628814..105458936hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg38830123
hg19830123
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18123351
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6407801
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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