A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6381948



Internal ID21039501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:46063901..46065000hg38UCSC Ensembl
chr4:46065918..46067017hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18117815
Samples
Known GenesGABRG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6381948
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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