A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6390277



Internal ID21047830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:155857801..155859279hg38UCSC Ensembl
chr4:156778953..156780431hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg381479
hg191479
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212139
Samples
Known GenesASIC5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6390277
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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