A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17377683



Internal ID22435553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:27791776..27791776hg38UCSC Ensembl
chr17:26118802..26118802hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38220
hg19220
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5973360
Supporting Variants
Samples
Known GenesNOS2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17377683
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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