A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv831n100



Internal ID22786918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46169941..46287904hg38UCSC Ensembl
chr10:47541177..47659140hg19UCSC Ensembl
chr10:47011183..47129146hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38117964
hg19117964
hg18117964
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1041495, nsv1042982, nsv1052967, nsv1055130, nsv1043372, nsv1050149, nsv1038301
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)dgv831n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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