A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6448975



Internal ID21106528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:25700412..25701369hg38UCSC Ensembl
chr10:25989341..25990298hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38958
hg19958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17979330
Samples
Known GenesLINC00836
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6448975
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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