A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589777



Internal ID16377186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:14667411..14704064hg38UCSC Ensembl
Innerchr3:14708918..14745571hg19UCSC Ensembl
Innerchr3:14683922..14720575hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3836654
hg1936654
hg1836654
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv959447
Samples
Known GenesC3orf20, CCDC174
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589777
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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