A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6530046



Internal ID20903407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:26700048..26700680hg38UCSC Ensembl
chr18:24280012..24280644hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38633
hg19633
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18039592
Samples
Known GenesLOC728606
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6530046
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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