A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6505965



Internal ID20879240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:65495301..65537900hg38UCSC Ensembl
chr15:65787639..65830238hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3842600
hg1942600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182553
Samples
Known GenesDPP8, PTPLAD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6505965
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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