A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6516825



Internal ID20890186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:37024578..37026753hg38UCSC Ensembl
chr18:34604541..34606716hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg382176
hg192176
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18040427
Samples
Known GenesKIAA1328
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6516825
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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