A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6496703



Internal ID20869906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:66397379..66397990hg38UCSC Ensembl
chr16:66431282..66431893hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38612
hg19612
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18031269
Samples
Known GenesCDH5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6496703
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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