A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6382591



Internal ID21040144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:174704018..174705819hg38UCSC Ensembl
chr4:175625169..175626970hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg381802
hg191802
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18113045
Samples
Known GenesGLRA3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6382591
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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