A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6323798



Internal ID20856920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:167891501..167897500hg38UCSC Ensembl
chr1:167860739..167866738hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg386000
hg196000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18201531
Samples
Known GenesADCY10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6323798
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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