A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169767



Internal ID21313578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:194274521..194370368hg38UCSC Ensembl
Outerchr1:194271276..194372476hg38UCSC Ensembl
Innerchr1:194243651..194339498hg19UCSC Ensembl
Outerchr1:194240406..194341606hg19UCSC Ensembl
Innerchr1:192510274..192606121hg18UCSC Ensembl
Outerchr1:192507029..192608229hg18UCSC Ensembl
Cytoband1q31.3
Allele length
AssemblyAllele length
hg38101201
hg19101201
hg18101201
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14244390
SamplesNGO_32
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169767
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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