A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2795069



Internal ID21240407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41031548..41031548hg38UCSC Ensembl
chr15:41323746..41323746hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13683415
Samples
Known GenesINO80
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2795069
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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