A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17475896



Internal ID22533794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:73220446..73221545hg38UCSC Ensembl
chr17:71216585..71217684hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5870374
Supporting Variants
Samples
Known GenesFAM104A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17475896
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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