A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv958046



Internal ID16960233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:89732738..89733052hg38UCSC Ensembl
Outerchr16:89799146..89799460hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3005661
SamplesBILGI_BIOE
Known GenesZNF276
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv958046
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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