A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449592



Internal ID21107145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:12182885..12184138hg38UCSC Ensembl
chr10:12224884..12226137hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg381254
hg191254
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17978184
Samples
Known GenesNUDT5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449592
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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