A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6440037



Internal ID21097590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:111105291..111112527hg38UCSC Ensembl
chr10:112865049..112872285hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg387237
hg197237
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17977848
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6440037
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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