A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6527563



Internal ID20900924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:39619012..39653498hg38UCSC Ensembl
chr18:37198976..37233462hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg3834487
hg1934487
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18040182
Samples
Known GenesLINC00669
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6527563
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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