A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv171n100



Internal ID20151787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:61973547..62006919hg38UCSC Ensembl
chr1:62439219..62472591hg19UCSC Ensembl
chr1:62211807..62245179hg18UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg3833373
hg1933373
hg1833373
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1005178, nsv999481
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)dgv171n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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