A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13705000



Internal ID21226803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:29451901..29451901hg38UCSC Ensembl
chr19:51555173..51555173hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg38118
hg19118
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2802810
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13705000
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency1


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