A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515277



Internal ID20888636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:10605613..10633236hg38UCSC Ensembl
chr16:10699470..10727093hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3827624
hg1927624
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18028280
Samples
Known GenesTEKT5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515277
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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