A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6527318



Internal ID20900679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:36373008..36375792hg38UCSC Ensembl
chr18:33952971..33955755hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg382785
hg192785
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18177653
Samples
Known GenesFHOD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6527318
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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