A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv682n100



Internal ID22786769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:19030782..19058141hg38UCSC Ensembl
chr10:19319711..19347070hg19UCSC Ensembl
chr10:19359717..19387076hg18UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3827360
hg1927360
hg1827360
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1049708, nsv1038358, nsv1043004
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)dgv682n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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