A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv958194



Internal ID16960381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:22897655..22897987hg38UCSC Ensembl
Outerchr16:22908976..22909308hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg38333
hg19333
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3005621
SamplesBILGI_BIOE
Known GenesHS3ST2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv958194
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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