A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6405295



Internal ID21062848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:4996607..4998672hg38UCSC Ensembl
chr6:4996841..4998906hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg382066
hg192066
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18143470
Samples
Known GenesRPP40
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6405295
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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