A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6384962



Internal ID21042515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:163695506..163729549hg38UCSC Ensembl
chr4:164616658..164650701hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg3834044
hg1934044
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18114405
Samples
Known GenesMARCH1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6384962
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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