A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv169n100



Internal ID20151785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:61970095..61981630hg38UCSC Ensembl
chr1:62435767..62447302hg19UCSC Ensembl
chr1:62208355..62219890hg18UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg3811536
hg1911536
hg1811536
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1004315, nsv1014528, nsv1009859, nsv997843
Samples
Known GenesINADL
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv169n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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