A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6366136



Internal ID21023689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:1609773..1643195hg38UCSC Ensembl
chr4:1611500..1644922hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3833423
hg1933423
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18113620
Samples
Known GenesFAM53A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6366136
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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