A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17513636



Internal ID22571592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:4604731..4608888hg38UCSC Ensembl
chr9:4604731..4608888hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg384158
hg194158
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5858875
Supporting Variants
Samples
Known GenesSPATA6L
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17513636
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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