A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6388909



Internal ID21046462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:164202054..164215351hg38UCSC Ensembl
chr4:165123206..165136503hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg3813298
hg1913298
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18114464
Samples
Known GenesMARCH1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6388909
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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