A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6443976



Internal ID21101529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:9192400..9196589hg38UCSC Ensembl
chr10:9234363..9238552hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg384190
hg194190
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17985381
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6443976
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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