A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4084n100



Internal ID22790171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:141408063..141477739hg38UCSC Ensembl
chr2:142165632..142235308hg19UCSC Ensembl
chr2:141882102..141951778hg18UCSC Ensembl
Cytoband2q22.1
Allele length
AssemblyAllele length
hg3869677
hg1969677
hg1869677
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1002208, nsv1009183
Samples
Known GenesLRP1B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4084n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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