A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18201531



Internal ID20768572
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 StatusS
Merged Variantsnsv6323798
Supporting Variants
Samples
Known GenesADCY10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18201531
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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