A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17471110



Internal ID22529001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:29179436..29182150hg38UCSC Ensembl
chr15:29471639..29474353hg19UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg382715
hg192715
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5865653
Supporting Variants
Samples
Known GenesFAM189A1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17471110
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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