A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6332984



Internal ID20866159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:10007210..10057075hg38UCSC Ensembl
chr1:10067268..10117133hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg3849866
hg1949866
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18200284
Samples
Known GenesRBP7, UBE4B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6332984
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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