A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6528658



Internal ID20902019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:55627701..55632571hg38UCSC Ensembl
chr18:53294932..53299802hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg384871
hg194871
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18042508
Samples
Known GenesTCF4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6528658
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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