A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6407470



Internal ID21065023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:81800006..81801994hg38UCSC Ensembl
chr5:81095825..81097813hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg381989
hg191989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18132926
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6407470
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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