A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15191636



Internal ID21330499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:59225143..59225143hg38UCSC Ensembl
chr10:60984903..60984903hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38329
hg19329
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3942429
Supporting Variants
SamplesHG002
Known GenesPHYHIPL
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15191636
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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