A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6327162



Internal ID20860299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:205034793..205037466hg38UCSC Ensembl
chr1:205003921..205006594hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg382674
hg192674
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18057032
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6327162
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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