A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6520188



Internal ID20893549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:14769601..14772500hg38UCSC Ensembl
chr18:14769600..14772499hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg382900
hg192900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18039377
Samples
Known GenesANKRD30B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6520188
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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