A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6524026



Internal ID20897387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:4181993..4182418hg38UCSC Ensembl
chr18:4181993..4182418hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg38426
hg19426
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18041808
Samples
Known GenesDLGAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6524026
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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