A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv957725



Internal ID16959912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:69163026..69163363hg38UCSC Ensembl
Outerchr9:71777942..71778279hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg38338
hg19338
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3002335
SamplesBILGI_BIOE
Known GenesTJP2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv957725
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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