A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18038739



Internal ID20605779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:11855906..11857123hg38UCSC Ensembl
chr18:11855905..11857122hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg381218
hg191218
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6524988
Supporting Variants
Samples
Known GenesGNAL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18038739
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00586


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