A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6328229



Internal ID20861374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:195307049..195468332hg38UCSC Ensembl
chr1:195276179..195437462hg19UCSC Ensembl
Cytoband1q31.3
Allele length
AssemblyAllele length
hg38161284
hg19161284
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18056139
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6328229
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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