A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17468908



Internal ID22526798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:37105381..37108515hg38UCSC Ensembl
chr13:37679518..37682652hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg383135
hg193135
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5866930
Supporting Variants
Samples
Known GenesCSNK1A1L
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17468908
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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