A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6436871



Internal ID21094424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:126454434..126461427hg38UCSC Ensembl
chr10:128143003..128149996hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg386994
hg196994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17978680
Samples
Known GenesC10orf90
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6436871
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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