A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2814607



Internal ID21259945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:73205684..73205684hg38UCSC Ensembl
chr6:73915407..73915407hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13704222
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2814607
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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