A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6497127



Internal ID20870331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:72700667..72704104hg38UCSC Ensembl
chr15:72993008..72996445hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg383438
hg193438
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18026597
Samples
Known GenesBBS4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6497127
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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