A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6373771



Internal ID21031324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:15068727..15069373hg38UCSC Ensembl
chr4:15070351..15070997hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg38647
hg19647
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18112880
Samples
Known GenesCPEB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6373771
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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