A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6321518



Internal ID20854624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:204639690..204640683hg38UCSC Ensembl
chr1:204608818..204609811hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg38994
hg19994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18057019
Samples
Known GenesLRRN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6321518
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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