A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6500708



Internal ID20873936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:61739324..61751711hg38UCSC Ensembl
chr16:61773228..61785615hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3812388
hg1912388
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18030795
Samples
Known GenesCDH8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6500708
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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