A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6514696



Internal ID20888051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:88886298..88886829hg38UCSC Ensembl
chr15:89429529..89430060hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38532
hg19532
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18027012
Samples
Known GenesHAPLN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6514696
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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