A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6385876



Internal ID21043429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:164109723..164171825hg38UCSC Ensembl
chr4:165030875..165092977hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg3862103
hg1962103
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213771
Samples
Known GenesMARCH1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6385876
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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