A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18144144



Internal ID20711184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:45177513..45318065hg38UCSC Ensembl
chr6:45145250..45285802hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38140553
hg19140553
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6401677
Supporting Variants
Samples
Known GenesMIR586, SUPT3H
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18144144
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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