A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6439863



Internal ID21097416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:37648767..37652233hg38UCSC Ensembl
chr10:37937695..37941161hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg383467
hg193467
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17979928
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6439863
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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