A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6445625



Internal ID21103178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:21287347..21288279hg38UCSC Ensembl
chr10:21576276..21577208hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38933
hg19933
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17979150
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6445625
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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