A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17500332



Internal ID22558269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:171913882..171927683hg38UCSC Ensembl
chr4:172835033..172848834hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg3813802
hg1913802
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5838433
Supporting Variants
Samples
Known GenesGALNTL6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17500332
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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