A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6439159



Internal ID21096712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:104269124..104282063hg38UCSC Ensembl
chr10:106028882..106041821hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg3812940
hg1912940
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17977740
Samples
Known GenesGSTO2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6439159
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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