A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2795262



Internal ID21240600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:60350048..60350048hg38UCSC Ensembl
chr15:60642247..60642247hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38162
hg19162
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13687434
Samples
Known GenesANXA2
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2795262
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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