A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv958050



Internal ID16960237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:66379951..66380241hg38UCSC Ensembl
Outerchr16:66413854..66414144hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38291
hg19291
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3005665
SamplesBILGI_BIOE
Known GenesCDH5
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv958050
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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