A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6385296



Internal ID21042849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:139083001..139084900hg38UCSC Ensembl
chr4:140004155..140006054hg19UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213031
Samples
Known GenesELF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6385296
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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