A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2814612



Internal ID21259950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:75924658..75924658hg38UCSC Ensembl
chr6:76634375..76634375hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13698275
Samples
Known GenesIMPG1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2814612
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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