A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6386047



Internal ID21043600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:54481229..54484195hg38UCSC Ensembl
chr4:55347396..55350362hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg382967
hg192967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18117690
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6386047
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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