A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6442736



Internal ID21100289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:21113397..21113996hg38UCSC Ensembl
chr10:21402326..21402925hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38600
hg19600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17979141
Samples
Known GenesNEBL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6442736
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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