A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17352377



Internal ID22578046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:59225143..59225143hg38UCSC Ensembl
chr10:60984903..60984903hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5948804
Supporting Variants
Samples
Known GenesPHYHIPL
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17352377
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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