A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv466n100



Internal ID20152082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:175459821..175796653hg38UCSC Ensembl
chr1:175428957..175765789hg19UCSC Ensembl
chr1:173695580..174032412hg18UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg38336833
hg19336833
hg18336833
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1000135, nsv999586, nsv1014015, nsv1008727, nsv998119, nsv1012012, nsv1011962, nsv1008620, nsv1004585
Samples
Known GenesTNR
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv466n100
Frequency
Sample Size29084
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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