A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17476304



Internal ID22534202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:15088250..15096049hg38UCSC Ensembl
chr16:15182107..15189906hg19UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg387800
hg197800
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5873911
Supporting Variants
Samples
Known GenesPDXDC1, RRN3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17476304
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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