A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6514194



Internal ID20887546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:10554319..10555838hg38UCSC Ensembl
chr16:10648176..10649695hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg381520
hg191520
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18028273
Samples
Known GenesEMP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6514194
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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