A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6523595



Internal ID20896956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:23613541..23614330hg38UCSC Ensembl
chr18:21193505..21194294hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38790
hg19790
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18040375
Samples
Known GenesANKRD29
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6523595
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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