A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14244673



Internal ID21303659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:134487789..134488918hg38UCSC Ensembl
Outerchr9:134483927..134495183hg38UCSC Ensembl
Innerchr9:137379635..137380764hg19UCSC Ensembl
Outerchr9:137375773..137387029hg19UCSC Ensembl
Innerchr9:136519456..136520585hg18UCSC Ensembl
Outerchr9:136515594..136526850hg18UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg3811257
hg1911257
hg1811257
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169619
Supporting Variants
SamplesMLY_8
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14244673
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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