A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2795372



Internal ID21240710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:74894108..74894108hg38UCSC Ensembl
chr15:75186449..75186449hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13681653
Samples
Known GenesMPI
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2795372
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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