A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6510907



Internal ID20884230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:81030501..81039200hg38UCSC Ensembl
chr16:81064106..81072805hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg388700
hg198700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18194872
Samples
Known GenesATMIN, CENPN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6510907
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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