A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6517399



Internal ID20890760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:30298401..30299700hg38UCSC Ensembl
chr18:27878367..27879666hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18039706
Samples
Known GenesMIR302F
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6517399
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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