A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2814542



Internal ID21259880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:44042417..44042417hg38UCSC Ensembl
chr6:44010154..44010154hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13702249
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2814542
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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