A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169507



Internal ID21313740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:3862706..4142615hg38UCSC Ensembl
Outerchr3:3859793..4143342hg38UCSC Ensembl
Innerchr3:3904390..4184299hg19UCSC Ensembl
Outerchr3:3901477..4185026hg19UCSC Ensembl
Innerchr3:3879390..4159299hg18UCSC Ensembl
Outerchr3:3876477..4160026hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38283550
hg19283550
hg18283550
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14247585, nssv14243063
SamplesMLY_1, SNI_11
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169507
Frequency
Sample Size93
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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