A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2796606



Internal ID21241944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:131150..131150hg38UCSC Ensembl
chr11:186391..186391hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38343
hg19343
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13687132
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2796606
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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