A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169714



Internal ID21313525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:127405942..127458097hg38UCSC Ensembl
Outerchr9:127399371..127459109hg38UCSC Ensembl
Innerchr9:130168221..130220376hg19UCSC Ensembl
Outerchr9:130161650..130221388hg19UCSC Ensembl
Innerchr9:129208042..129260197hg18UCSC Ensembl
Outerchr9:129201471..129261209hg18UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3859739
hg1959739
hg1859739
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14242028
SamplesNGO_23
Known GenesLRSAM1, RPL12, SLC2A8, SNORA65, ZNF79
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169714
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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