A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6329314



Internal ID20862466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:119056342..119060644hg38UCSC Ensembl
chr1:119598965..119603267hg19UCSC Ensembl
Cytoband1p12
Allele length
AssemblyAllele length
hg384303
hg194303
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18051240
Samples
Known GenesWARS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6329314
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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