A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6529771



Internal ID20903132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:29354846..29359968hg38UCSC Ensembl
chr18:26934811..26939933hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg385123
hg195123
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18040936
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6529771
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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