A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6328378



Internal ID20861526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:9999329..10000010hg38UCSC Ensembl
chr1:10059387..10060068hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg38682
hg19682
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202152
Samples
Known GenesRBP7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6328378
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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