A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6439280



Internal ID21096833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:68143962..68145231hg38UCSC Ensembl
chr10:69903719..69904988hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg381270
hg191270
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17982997
Samples
Known GenesMYPN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6439280
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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