A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6474837



Internal ID21132390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:88044630..88053574hg38UCSC Ensembl
chr11:87777798..87786742hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg388945
hg198945
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17995013
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6474837
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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