A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6517262



Internal ID20890623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:48252018..48256427hg38UCSC Ensembl
chr18:45778389..45782798hg19UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg384410
hg194410
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18042004
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6517262
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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