A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6023297



Internal ID21932640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:76288895..78160088hg38UCSC Ensembl
chr18:74000850..75920088hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg381871194
hg191919239
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17635335
Samples
Known GenesFLJ44313, GALR1, LINC00908, LINC01029, LOC100131655, MBP, ZNF236, ZNF516
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6023297
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer