A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv251n100



Internal ID20151867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:108930151..108955511hg38UCSC Ensembl
chr1:109472773..109498133hg19UCSC Ensembl
chr1:109274296..109299656hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3825361
hg1925361
hg1825361
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1000677, nsv1001314
Samples
Known GenesCLCC1, GPSM2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv251n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer