A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6386640



Internal ID21044193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:147603539..147659052hg38UCSC Ensembl
chr4:148524690..148580203hg19UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg3855514
hg1955514
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18109604
Samples
Known GenesPRMT10, TMEM184C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6386640
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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