A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6398862



Internal ID21056415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:13694624..13695373hg38UCSC Ensembl
chr6:13694856..13695605hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg38750
hg19750
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18138315
Samples
Known GenesRANBP9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6398862
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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