A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6328622



Internal ID20861770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:156613128..156618501hg38UCSC Ensembl
chr1:156582920..156588293hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg385374
hg195374
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18052274
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6328622
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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