A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15191736



Internal ID21330601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:123881229..123881229hg38UCSC Ensembl
chr10:125640745..125640745hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3948693
Supporting Variants
SamplesHG002
Known GenesCPXM2
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15191736
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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