A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449998



Internal ID21107551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:102855159..102861970hg38UCSC Ensembl
chr10:104614916..104621727hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg386812
hg196812
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17977279
Samples
Known GenesC10orf32, C10orf32-ASMT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449998
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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