A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13689229



Internal ID21211081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:165708195..165708195hg38UCSC Ensembl
chr1:165677432..165677432hg19UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2801055
Supporting Variants
Samples
Known GenesLOC440700
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13689229
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.571429


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