A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515725



Internal ID20889086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:9168092..9181572hg38UCSC Ensembl
chr18:9168090..9181570hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg3813481
hg1913481
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18044359
Samples
Known GenesANKRD12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515725
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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