A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6411274



Internal ID21068827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:56462246..56472419hg38UCSC Ensembl
chr5:55758073..55768246hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3810174
hg1910174
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18131804
Samples
Known GenesLOC102467147
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6411274
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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