A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6517034



Internal ID20890395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:26876564..26877162hg38UCSC Ensembl
chr18:24456528..24457126hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38599
hg19599
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18039806
Samples
Known GenesAQP4-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6517034
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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