A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6381264



Internal ID21038817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:153338354..153367016hg38UCSC Ensembl
chr4:154259506..154288168hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3828663
hg1928663
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212111
Samples
Known GenesMND1, TRIM2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6381264
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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