A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6317525



Internal ID20850612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:52885370..52886135hg38UCSC Ensembl
chr1:53351042..53351807hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg38766
hg19766
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18201457
Samples
Known GenesZYG11A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6317525
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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