A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6530177



Internal ID20903538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:27053401..27055700hg38UCSC Ensembl
chr18:24633365..24635664hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg382300
hg192300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18039814
Samples
Known GenesCHST9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6530177
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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