A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10n100



Internal ID20151626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:1779975..1884542hg38UCSC Ensembl
chr1:1711414..1815981hg19UCSC Ensembl
chr1:1701274..1805841hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg38104568
hg19104568
hg18104568
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1011008, nsv1007257
Samples
Known GenesGNB1, NADK
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv10n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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