A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170142



Internal ID21314203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:64802989..64817240hg38UCSC Ensembl
Outerchr14:64801887..64817321hg38UCSC Ensembl
Innerchr14:65269707..65283958hg19UCSC Ensembl
Outerchr14:65268605..65284039hg19UCSC Ensembl
Innerchr14:64339460..64353711hg18UCSC Ensembl
Outerchr14:64338358..64353792hg18UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg3815435
hg1915435
hg1815435
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14244978
SamplesNGO_25
Known GenesSPTB
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3170142
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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