A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6507375



Internal ID20880665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:50893895..51071954hg38UCSC Ensembl
chr15:51186092..51364151hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg38178060
hg19178060
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18025215
Samples
Known GenesAP4E1, DCAF13P3, TNFAIP8L3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6507375
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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