A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3002326



Internal ID16948592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:17277061..17277298hg38UCSC Ensembl
Outerchr9:17277059..17277296hg19UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg38238
hg19238
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv957716
Supporting Variants
SamplesBILGI_BIOE
Known GenesCNTLN
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3002326
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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