A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6527396



Internal ID20900757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:3421958..3423406hg38UCSC Ensembl
chr18:3421956..3423404hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg381449
hg191449
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18040997
Samples
Known GenesTGIF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6527396
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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