A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6426707



Internal ID21084260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:30496256..30497631hg38UCSC Ensembl
chr8:30353773..30355148hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg381376
hg191376
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18165850
Samples
Known GenesRBPMS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6426707
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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