A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4998n100



Internal ID22791085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:177685633..177707860hg38UCSC Ensembl
chr3:177403421..177425648hg19UCSC Ensembl
chr3:178886115..178908342hg18UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg3822228
hg1922228
hg1822228
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1009087, nsv998537
Samples
Known GenesLINC00578
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4998n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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