A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6385061



Internal ID21042614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:163691201..163699100hg38UCSC Ensembl
chr4:164612353..164620252hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg387900
hg197900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18114402
Samples
Known GenesMARCH1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6385061
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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