A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3139n100



Internal ID22789226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:33306183..33352174hg38UCSC Ensembl
chr17:31633201..31679192hg19UCSC Ensembl
chr17:28657314..28703305hg18UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg3845992
hg1945992
hg1845992
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1062804, nsv1055797
Samples
Known GenesASIC2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3139n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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