A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6387707



Internal ID21045260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:138334600..138340720hg38UCSC Ensembl
chr4:139255754..139261874hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg386121
hg196121
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18111522
Samples
Known GenesLINC00499
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6387707
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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