A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515567



Internal ID20888927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:84575554..84608526hg38UCSC Ensembl
chr15:85118785..85151757hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg3832973
hg1932973
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180226
Samples
Known GenesLINC00933, ZSCAN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515567
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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