A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17473091



Internal ID22530983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:32060413..32064923hg38UCSC Ensembl
chr17:30387432..30391942hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg384511
hg194511
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5877749
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17473091
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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