A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13677526



Internal ID21199336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:11509265..11509265hg38UCSC Ensembl
chr18:11509264..11509264hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38184
hg19184
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2797673
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13677526
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.5625


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