A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17474865



Internal ID22532760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:11291219..11292894hg38UCSC Ensembl
chr17:11194536..11196211hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg381676
hg191676
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5878748
Supporting Variants
Samples
Known GenesSHISA6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17474865
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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