A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6329498



Internal ID20862650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:26288435..26300144hg38UCSC Ensembl
chr1:26614926..26626635hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3811710
hg1911710
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18060576
Samples
Known GenesUBXN11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6329498
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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