A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170222



Internal ID21314283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:153701198..153720772hg38UCSC Ensembl
Outerchr1:153699771..153722864hg38UCSC Ensembl
Innerchr1:153673674..153693248hg19UCSC Ensembl
Outerchr1:153672247..153695340hg19UCSC Ensembl
Innerchr1:151940298..151959872hg18UCSC Ensembl
Outerchr1:151938871..151961964hg18UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3823094
hg1923094
hg1823094
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14245524, nssv14247717
SamplesNGO_53, NGO_43
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3170222
Frequency
Sample Size93
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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