A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6512691



Internal ID20886028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:62155101..62229800hg38UCSC Ensembl
chr15:62447300..62521999hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3874700
hg1974700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18195872
Samples
Known GenesC2CD4B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6512691
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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