A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6533049



Internal ID20906410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:26977701..26992200hg38UCSC Ensembl
chr18:24557665..24572164hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg3814500
hg1914500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18039811
Samples
Known GenesCHST9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6533049
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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