A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2813491



Internal ID21258829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:148178724..148178724hg38UCSC Ensembl
chr6:148499860..148499860hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13709912
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2813491
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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