A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6522671



Internal ID20896032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:11688701..11690300hg38UCSC Ensembl
chr18:11688700..11690299hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18038725
Samples
Known GenesGNAL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6522671
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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