A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6510767



Internal ID20884089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:52096885..52138128hg38UCSC Ensembl
chr15:52389082..52430325hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3841244
hg1941244
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18024052
Samples
Known GenesBCL2L10, GNB5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6510767
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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