A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6334925



Internal ID20868114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:24680368..24685171hg38UCSC Ensembl
chr1:25006859..25011662hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg384804
hg194804
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18059872
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6334925
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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