A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6444015



Internal ID21101568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:43066772..43073930hg38UCSC Ensembl
chr10:43562220..43569378hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg387159
hg197159
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17980224
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6444015
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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