A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6316298



Internal ID20849377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:202074171..202083859hg38UCSC Ensembl
chr1:202043299..202052987hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg389689
hg199689
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18201818
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6316298
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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