A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170090



Internal ID21314151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:24202763..24204879hg38UCSC Ensembl
Outerchr14:24199204..24211720hg38UCSC Ensembl
Innerchr14:24671969..24674085hg19UCSC Ensembl
Outerchr14:24668410..24680926hg19UCSC Ensembl
Innerchr14:23741809..23743925hg18UCSC Ensembl
Outerchr14:23738250..23750766hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3812517
hg1912517
hg1812517
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14251590
SamplesNGO_53
Known GenesCHMP4A, TSSK4
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3170090
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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