A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6327745



Internal ID20860887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:151073317..151073811hg38UCSC Ensembl
chr1:151045793..151046287hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38495
hg19495
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18053016
Samples
Known GenesGABPB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6327745
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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