A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169946



Internal ID21314007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:9813820..9839756hg38UCSC Ensembl
Outerchr2:9810242..9844047hg38UCSC Ensembl
Innerchr2:9953949..9979885hg19UCSC Ensembl
Outerchr2:9950371..9984176hg19UCSC Ensembl
Innerchr2:9871400..9897336hg18UCSC Ensembl
Outerchr2:9867822..9901627hg18UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg3833806
hg1933806
hg1833806
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14248336
SamplesNGO_32
Known GenesTAF1B
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169946
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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