A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6445933



Internal ID21103486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:8147890..8149332hg38UCSC Ensembl
chr10:8189853..8191295hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg381443
hg191443
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17984740
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6445933
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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