A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6496314



Internal ID20869514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:11340601..11383453hg38UCSC Ensembl
chr16:11434458..11477310hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3842853
hg1942853
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18028334
Samples
Known GenesRMI2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6496314
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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