A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6326286



Internal ID20859420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:11081990..11083408hg38UCSC Ensembl
chr1:11142047..11143465hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg381419
hg191419
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18050871
Samples
Known GenesEXOSC10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6326286
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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