A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6429572



Internal ID21087125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:87228001..87229600hg38UCSC Ensembl
chr8:88240229..88241828hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227457
Samples
Known GenesCNBD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6429572
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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