A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952072



Internal ID16954259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:89032193..89201992hg38UCSC Ensembl
Outerchr16:89098601..89268400hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38169800
hg19169800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3000191
SamplesBILGI_BIOE
Known GenesACSF3, CDH15, LINC00304, LOC400558, SLC22A31
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952072
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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