A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6437623



Internal ID21095176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1139335..2146715hg38UCSC Ensembl
chr10:1185275..2188909hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg381007381
hg191003635
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180930
Samples
Known GenesADARB2, ADARB2-AS1, LINC00200, LINC00700, MIR6072
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6437623
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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