A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169401



Internal ID21313884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:212656702..212707890hg38UCSC Ensembl
Outerchr1:212655717..212712463hg38UCSC Ensembl
Innerchr1:212830044..212881232hg19UCSC Ensembl
Outerchr1:212829059..212885805hg19UCSC Ensembl
Innerchr1:210896667..210947855hg18UCSC Ensembl
Outerchr1:210895682..210952428hg18UCSC Ensembl
Cytoband1q32.3
Allele length
AssemblyAllele length
hg3856747
hg1956747
hg1856747
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14249981
SamplesNGO_25
Known GenesBATF3
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169401
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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