A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv889150



Internal ID15836420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:79521227..79522270hg38UCSC Ensembl
Innerchr18:77281227..77282270hg19UCSC Ensembl
Innerchr18:75382215..75383258hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg381044
hg191044
hg181044
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv577886
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)nssv889150
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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