A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6325707



Internal ID20858839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:114263654..114264039hg38UCSC Ensembl
chr1:114806276..114806661hg19UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg38386
hg19386
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18051630
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6325707
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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