A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17474387



Internal ID22532281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:44811962..44814651hg38UCSC Ensembl
chr17:42889330..42892019hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg382690
hg192690
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5870668
Supporting Variants
Samples
Known GenesGJC1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17474387
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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