A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6455379



Internal ID21112932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:81046835..81047277hg38UCSC Ensembl
chr10:82806591..82807033hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg38443
hg19443
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17983654
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6455379
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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