A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13677914



Internal ID21199751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:136266..136326hg38UCSC Ensembl
chr11:191801..191857hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3861
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2796995
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13677914
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency1


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