A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv125n100



Internal ID20151741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:16912960..16931436hg38UCSC Ensembl
chr1:17239455..17257931hg19UCSC Ensembl
chr1:17112042..17130518hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3818477
hg1918477
hg1818477
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1010177, nsv1014417, nsv1008214
Samples
Known GenesCROCC
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv125n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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