A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6387370



Internal ID21044923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:79087862..79091742hg38UCSC Ensembl
chr4:80009016..80012896hg19UCSC Ensembl
Cytoband4q21.21
Allele length
AssemblyAllele length
hg383881
hg193881
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18120389
Samples
Known GenesLINC01088
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6387370
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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