A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv176n100



Internal ID22786263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:69683011..69716895hg38UCSC Ensembl
chr1:70148694..70182578hg19UCSC Ensembl
chr1:69921282..69955166hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3833885
hg1933885
hg1833885
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv998121, nsv1010921
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv176n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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