A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6530959



Internal ID20904320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:50807815..50808875hg38UCSC Ensembl
chr18:48334185..48335245hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg381061
hg191061
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18042215
Samples
Known GenesMRO
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6530959
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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