A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv889145



Internal ID15836415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:79439478..79481665hg38UCSC Ensembl
Innerchr18:77199478..77241665hg19UCSC Ensembl
Innerchr18:75300466..75342653hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3842188
hg1942188
hg1842188
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv577881
Supporting Variants
Samples
Known GenesNFATC1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv889145
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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