A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6424676



Internal ID21082229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:27770325..27776126hg38UCSC Ensembl
chr8:27627842..27633643hg19UCSC Ensembl
Cytoband8p21.1
Allele length
AssemblyAllele length
hg385802
hg195802
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232026
Samples
Known GenesCCDC25, ESCO2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6424676
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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