A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6406996



Internal ID21064549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:57108201..57109900hg38UCSC Ensembl
chr5:56404028..56405727hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18131295
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6406996
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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