A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13693573



Internal ID21215423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:121795802..121795802hg38UCSC Ensembl
chr1:121424254..121424254hg19UCSC Ensembl
Cytoband1p11.2
Allele length
AssemblyAllele length
hg38337
hg19337
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2800446
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13693573
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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