A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6319728



Internal ID20852824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:183155279..183161024hg38UCSC Ensembl
chr1:183124414..183130159hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg385746
hg195746
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18054690
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6319728
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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