A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6316100



Internal ID20849177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:18383485..18384678hg38UCSC Ensembl
chr1:18709979..18711172hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg381194
hg191194
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18054724
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6316100
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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