A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6513036



Internal ID20886376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89607402..89702833hg38UCSC Ensembl
chr16:89673810..89769241hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3895432
hg1995432
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18187912
Samples
Known GenesCDK10, CHMP1A, DPEP1, SPATA2L, SPATA33
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6513036
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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