A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6335335



Internal ID20868527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:202332101..202341300hg38UCSC Ensembl
chr1:202301229..202310428hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg389200
hg199200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18056682
Samples
Known GenesUBE2T
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6335335
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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