A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6377531



Internal ID21035084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:158768201..158769900hg38UCSC Ensembl
chr4:159689353..159691052hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212759
Samples
Known GenesFNIP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6377531
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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