A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13684998



Internal ID21206854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:84756772..84756772hg38UCSC Ensembl
chr1:85222455..85222455hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg38200
hg19200
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2801703
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13684998
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency1


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