A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170134



Internal ID21314195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:157395123..157439287hg38UCSC Ensembl
Outerchr2:157389591..157442735hg38UCSC Ensembl
Innerchr2:158251635..158295799hg19UCSC Ensembl
Outerchr2:158246103..158299247hg19UCSC Ensembl
Innerchr2:157959881..158004045hg18UCSC Ensembl
Outerchr2:157954349..158007493hg18UCSC Ensembl
Cytoband2q24.1
Allele length
AssemblyAllele length
hg3853145
hg1953145
hg1853145
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14245949
SamplesPML_1
Known GenesCYTIP
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3170134
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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