A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6507935



Internal ID20881231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:35469015..35470090hg38UCSC Ensembl
chr15:35761216..35762291hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg381076
hg191076
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18023399
Samples
Known GenesDPH6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6507935
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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