A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17363329



Internal ID22588998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:3752762..3752762hg38UCSC Ensembl
chr10:3794954..3794954hg19UCSC Ensembl
Cytoband10p15.2
Allele length
AssemblyAllele length
hg38290
hg19290
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5960313
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17363329
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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