A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6322867



Internal ID20855982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:244322905..244325260hg38UCSC Ensembl
chr1:244486207..244488562hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg382356
hg192356
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18059628
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6322867
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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