A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3002353



Internal ID16948619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:109667928..109668224hg38UCSC Ensembl
Outerchr9:112430208..112430504hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg38297
hg19297
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv957747
Supporting Variants
SamplesBILGI_BIOE
Known GenesPALM2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3002353
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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