A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv118n100



Internal ID20151734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:16886207..16949734hg38UCSC Ensembl
chr1:17212702..17276229hg19UCSC Ensembl
chr1:17085289..17148816hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3863528
hg1963528
hg1863528
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv997739, nsv1000008
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)dgv118n100
Frequency
Sample Size29084
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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