A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6400258



Internal ID21057811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:13635853..13636502hg38UCSC Ensembl
chr6:13636085..13636734hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg38650
hg19650
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18140125
Samples
Known GenesRANBP9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6400258
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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