A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2814934



Internal ID21260272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:42936146..42936146hg38UCSC Ensembl
chr6:42903884..42903884hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13704193
Samples
Known GenesCNPY3
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2814934
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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