A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6529034



Internal ID20902395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:48430870..48431486hg38UCSC Ensembl
chr18:45957241..45957857hg19UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg38617
hg19617
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18042015
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6529034
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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