A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170288



Internal ID21314349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:145858153..145898065hg38UCSC Ensembl
Outerchr3:145857256..145901677hg38UCSC Ensembl
Innerchr3:145575940..145615852hg19UCSC Ensembl
Outerchr3:145575043..145619464hg19UCSC Ensembl
Innerchr3:147058630..147098542hg18UCSC Ensembl
Outerchr3:147057733..147102154hg18UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3844422
hg1944422
hg1844422
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14250171
SamplesNGO_21
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3170288
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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