A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6496560



Internal ID20869763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:26748381..26749095hg38UCSC Ensembl
chr15:26993528..26994242hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg38715
hg19715
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18023697
Samples
Known GenesGABRB3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6496560
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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