A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6451900



Internal ID21109453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:72110516..72112497hg38UCSC Ensembl
chr10:73870274..73872255hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg381982
hg191982
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17983790
Samples
Known GenesASCC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6451900
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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