A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2999201



Internal ID16945467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:2817200..2863199hg38UCSC Ensembl
Outerchr16:2867201..2913200hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3846000
hg1946000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv952905
Supporting Variants
SamplesBILGI_BIOE
Known GenesPRSS21, PRSS22, PRSS30P, ZG16B
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2999201
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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