A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6376609



Internal ID21034162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:47875601..47879300hg38UCSC Ensembl
chr4:47877618..47881317hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg383700
hg193700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18117251
Samples
Known GenesNFXL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6376609
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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