A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6411470



Internal ID21069023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:73116412..73119323hg38UCSC Ensembl
chr5:72412239..72415150hg19UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg382912
hg192912
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18132187
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6411470
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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