A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17455368



Internal ID22513245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:155821776..155823575hg38UCSC Ensembl
chr1:155791567..155793366hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5828159
Supporting Variants
Samples
Known GenesGON4L
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17455368
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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