A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515436



Internal ID20888796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:23112391..23113833hg38UCSC Ensembl
chr16:23123712..23125154hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg381443
hg191443
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18028918
Samples
Known GenesUSP31
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515436
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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