A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6432576



Internal ID21090129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:70321300..70407934hg38UCSC Ensembl
chr8:71233535..71320169hg19UCSC Ensembl
Cytoband8q13.3
Allele length
AssemblyAllele length
hg3886635
hg1986635
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228019
Samples
Known GenesNCOA2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6432576
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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