A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6329114



Internal ID20862265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:18111677..18121587hg38UCSC Ensembl
chr1:18438171..18448081hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg389911
hg199911
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18054618
Samples
Known GenesIGSF21
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6329114
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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