A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170184



Internal ID21314245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:82112819..82177185hg38UCSC Ensembl
Outerchr2:82105406..82180692hg38UCSC Ensembl
Innerchr2:82339943..82404309hg19UCSC Ensembl
Outerchr2:82332530..82407816hg19UCSC Ensembl
Innerchr2:82193454..82257820hg18UCSC Ensembl
Outerchr2:82186041..82261327hg18UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg3875287
hg1975287
hg1875287
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14252150
SamplesNGO_32
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3170184
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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