A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6332648



Internal ID20865821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:198934740..198943455hg38UCSC Ensembl
chr1:198903869..198912584hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg388716
hg198716
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18056850
Samples
Known GenesMIR181A1HG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6332648
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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