A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6446572



Internal ID21104125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:5381568..5387668hg38UCSC Ensembl
chr10:5423531..5429631hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg386101
hg196101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17980863
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6446572
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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