A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951705



Internal ID17300579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:38807604..38921103hg38UCSC Ensembl
Outerchr9:38807601..38921100hg19UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg38113500
hg19113500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999394
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951705
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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