A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6529674



Internal ID20903035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:4451701..4460500hg38UCSC Ensembl
chr18:4451701..4460500hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg388800
hg198800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18187910
Samples
Known GenesDLGAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6529674
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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