A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17376498



Internal ID22602167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:6793085..6793085hg38UCSC Ensembl
chr17:6696404..6696404hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5970013
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17376498
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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