A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6450496



Internal ID21108049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:31056336..31058805hg38UCSC Ensembl
chr10:31345265..31347734hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg382470
hg192470
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17981430
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6450496
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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