A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6382985



Internal ID21040538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:139115501..139121400hg38UCSC Ensembl
chr4:140036655..140042554hg19UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg385900
hg195900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213032
Samples
Known GenesELF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6382985
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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