A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6507343



Internal ID20880632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:10144159..11379723hg38UCSC Ensembl
chr16:10238016..11473580hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg381235565
hg191235565
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18181415
Samples
Known GenesATF7IP2, CIITA, CLEC16A, DEXI, EMP2, GRIN2A, NUBP1, PRM1, PRM2, PRM3, RMI2, SOCS1, TEKT5, TNP2, TVP23A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6507343
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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