A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv844n100



Internal ID19011212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46261921..46333389hg38UCSC Ensembl
chr10:47633157..47704625hg19UCSC Ensembl
chr10:47103163..47174631hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3871469
hg1971469
hg1871469
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1046814, nsv1041678, nsv1037449, nsv1043807
Samples
Known GenesANTXRL, ANTXRLP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv844n100
Frequency
Sample Size29084
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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