A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6512652



Internal ID20885989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:101119482..101519788hg38UCSC Ensembl
chr15:101659687..102059991hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38400307
hg19400305
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18186412
Samples
Known GenesCHSY1, LOC100507472, PCSK6, SNRPA1, VIMP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6512652
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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