A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv626027



Internal ID15849560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:86540064..86540830hg38UCSC Ensembl
Outerchr9:86534414..86542151hg38UCSC Ensembl
Innerchr9:89154979..89155745hg19UCSC Ensembl
Outerchr9:89149329..89157066hg19UCSC Ensembl
Innerchr9:88344799..88345565hg18UCSC Ensembl
Outerchr9:88339149..88346886hg18UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg387738
hg197738
hg187738
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv511418
Supporting Variants
Samples1
Known Genes
MethodSNP array
AnalysisAnalysis of HGMDFN090 by Illumina HumanOmni1 Quad SNP array
PlatformGPL8882
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv626027
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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