A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6323829



Internal ID20856951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:180896951..180898282hg38UCSC Ensembl
chr1:180866087..180867418hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg381332
hg191332
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18054609
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6323829
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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