A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv113n100



Internal ID20151729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:16876990..16934756hg38UCSC Ensembl
chr1:17203485..17261251hg19UCSC Ensembl
chr1:17076072..17133838hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3857767
hg1957767
hg1857767
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1003988, nsv1000445, nsv1009920, nsv1006577
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)dgv113n100
Frequency
Sample Size29084
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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