A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6510101



Internal ID20883416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:55519701..55521600hg38UCSC Ensembl
chr16:55553613..55555512hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18030180
Samples
Known GenesLPCAT2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6510101
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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