A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577884



Internal ID16018607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:79485000..79528806hg38UCSC Ensembl
Innerchr18:77245000..77288806hg19UCSC Ensembl
Innerchr18:75345988..75389794hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3843807
hg1943807
hg1843807
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6113n54
Supporting Variantsnssv889148
Samples
Known GenesNFATC1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577884
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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