A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6529656



Internal ID20903017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:42356422..42364037hg38UCSC Ensembl
chr18:39936387..39944002hg19UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg387616
hg197616
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18042068
Samples
Known GenesLINC00907
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6529656
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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