A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17363136



Internal ID22588805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6281166..6281166hg38UCSC Ensembl
chr10:6323129..6323129hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38272
hg19272
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5948770
Supporting Variants
Samples
Known GenesLOC399715
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17363136
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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