A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6454259



Internal ID21111812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:84287901..84312600hg38UCSC Ensembl
chr10:86047657..86072356hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3824700
hg1924700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17984590
Samples
Known GenesLINC00858
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6454259
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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