A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6434649



Internal ID21092202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:59829091..60217527hg38UCSC Ensembl
chr8:60741650..61130086hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg38388437
hg19388437
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223496
Samples
Known GenesCA8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6434649
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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