A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6521300



Internal ID20894661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:8733520..8736710hg38UCSC Ensembl
chr18:8733518..8736708hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg383191
hg193191
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18044330
Samples
Known GenesSOGA2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6521300
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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