A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6450822



Internal ID21108375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:35873253..35875058hg38UCSC Ensembl
chr10:36162181..36163986hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg381806
hg191806
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17979406
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6450822
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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