A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170032



Internal ID21314093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:41264421..41268750hg38UCSC Ensembl
Outerchr2:41261660..41275405hg38UCSC Ensembl
Innerchr2:41491561..41495890hg19UCSC Ensembl
Outerchr2:41488800..41502545hg19UCSC Ensembl
Innerchr2:41345065..41349394hg18UCSC Ensembl
Outerchr2:41342304..41356049hg18UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg3813746
hg1913746
hg1813746
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14251823
SamplesNGO_28
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3170032
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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