A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv742n100



Internal ID20152358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46467768..46878295hg38UCSC Ensembl
chr10:46674168..47081683hg19UCSC Ensembl
chr10:46094174..46501689hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38410528
hg19407516
hg18407516
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1050176, nsv1038611, nsv1035719, nsv1044911, nsv1050486, nsv1043778
Samples
Known GenesBMS1P1, BMS1P5, FAM35BP, FRMPD2P1, GLUD1P7, GPRIN2, SYT15
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv742n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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