A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6508186



Internal ID20881485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:29460764..29463413hg38UCSC Ensembl
chr15:29752968..29755617hg19UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg382650
hg192650
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18023805
Samples
Known GenesFAM189A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6508186
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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