A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6437130



Internal ID21094683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:98291756..98387459hg38UCSC Ensembl
chr10:100051513..100147216hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg3895704
hg1995704
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18190146
Samples
Known GenesPYROXD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6437130
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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