A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6507847



Internal ID20881143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89606701..89608600hg38UCSC Ensembl
chr15:90149932..90151831hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18026893
Samples
Known GenesTICRR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6507847
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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