A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6447675



Internal ID21105228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:80940855..80942366hg38UCSC Ensembl
chr10:82700611..82702122hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg381512
hg191512
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17983640
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6447675
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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