A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15179410



Internal ID21318206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:192857201..192857258hg38UCSC Ensembl
chr1:192826331..192826388hg19UCSC Ensembl
Cytoband1q31.2
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3940194
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15179410
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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