A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv112n100



Internal ID20151728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:16876990..16921891hg38UCSC Ensembl
chr1:17203485..17248386hg19UCSC Ensembl
chr1:17076072..17120973hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3844902
hg1944902
hg1844902
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1011785, nsv1005092, nsv1014469, nsv1006571, nsv1011411, nsv1004370, nsv1006185, nsv1004806, nsv1012168, nsv1006653
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv112n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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