A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169886



Internal ID21313697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:136513897..136562150hg38UCSC Ensembl
Outerchr2:136510305..136563525hg38UCSC Ensembl
Innerchr2:137271467..137319720hg19UCSC Ensembl
Outerchr2:137267875..137321095hg19UCSC Ensembl
Innerchr2:136987937..137036190hg18UCSC Ensembl
Outerchr2:136984345..137037565hg18UCSC Ensembl
Cytoband2q22.1
Allele length
AssemblyAllele length
hg3853221
hg1953221
hg1853221
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14251458
SamplesPML_2
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169886
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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