A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6526638



Internal ID20899999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:3411801..3412300hg38UCSC Ensembl
chr18:3411799..3412298hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg38500
hg19500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18040984
Samples
Known GenesTGIF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6526638
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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