A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6382161



Internal ID21039714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:37659515..37660138hg38UCSC Ensembl
chr4:37661137..37661760hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38624
hg19624
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213549
Samples
Known GenesRELL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6382161
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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