A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170116



Internal ID21314177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:6386382..6448440hg38UCSC Ensembl
Outerchr9:6383360..6455019hg38UCSC Ensembl
Innerchr9:6386382..6448440hg19UCSC Ensembl
Outerchr9:6383360..6455019hg19UCSC Ensembl
Innerchr9:6376382..6438440hg18UCSC Ensembl
Outerchr9:6373360..6445019hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3871660
hg1971660
hg1871660
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14252360
SamplesNGO_32
Known GenesUHRF2
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3170116
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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