A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13685620



Internal ID21207479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:214708884..214708884hg38UCSC Ensembl
chr1:214882227..214882227hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2801287
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13685620
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.078125


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