A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14240960



Internal ID21304084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:7180064..7436701hg38UCSC Ensembl
Outerchr18:7173517..7437606hg38UCSC Ensembl
Innerchr18:7180062..7436699hg19UCSC Ensembl
Outerchr18:7173515..7437604hg19UCSC Ensembl
Innerchr18:7170062..7426699hg18UCSC Ensembl
Outerchr18:7163515..7427604hg18UCSC Ensembl
Cytoband18p11.23
Allele length
AssemblyAllele length
hg38264090
hg19264090
hg18264090
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169461
Supporting Variants
SamplesNGO_10
Known GenesLRRC30
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14240960
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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