A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6325889



Internal ID20859022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:54439963..54443205hg38UCSC Ensembl
chr1:54905636..54908878hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg383243
hg193243
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18061546
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6325889
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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