A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6410936



Internal ID21068489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:163745148..163756704hg38UCSC Ensembl
chr5:163172154..163183710hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3811557
hg1911557
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18128449
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6410936
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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