A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6501197



Internal ID20874429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:30150403..30158270hg38UCSC Ensembl
chr16:30161724..30169591hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg387868
hg197868
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18029147
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6501197
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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