A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6367196



Internal ID21024749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:15066901..15069700hg38UCSC Ensembl
chr4:15068525..15071324hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg382800
hg192800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18112877
Samples
Known GenesCPEB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6367196
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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