A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6325412



Internal ID20858543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:40159521..40160177hg38UCSC Ensembl
chr1:40625193..40625849hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg38657
hg19657
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203095
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6325412
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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