A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17635335



Internal ID21827382
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 StatusS
Merged Variantsnsv6023297
Supporting Variants
Samples
Known GenesFLJ44313, GALR1, LINC00908, LINC01029, LOC100131655, MBP, ZNF236, ZNF516
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17635335
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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