A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18052092



Internal ID20619132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:155768665..155769585hg38UCSC Ensembl
chr1:155738456..155739376hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg38921
hg19921
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6333668
Supporting Variants
Samples
Known GenesGON4L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18052092
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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