A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6497237



Internal ID20870442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:9993547..10430792hg38UCSC Ensembl
chr16:10087404..10524649hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg38437246
hg19437246
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18194582
Samples
Known GenesATF7IP2, GRIN2A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6497237
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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