A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17478231



Internal ID22536132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:39160163..39168201hg38UCSC Ensembl
chr17:37316416..37324454hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg388039
hg198039
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5869895
Supporting Variants
Samples
Known GenesARL5C
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17478231
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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