A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15188870



Internal ID21327711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:180888413..180888413hg38UCSC Ensembl
chr1:180857549..180857549hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3944123
Supporting Variants
SamplesHG002
Known GenesXPR1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15188870
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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