A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv692n100



Internal ID22786779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:24088733..24099486hg38UCSC Ensembl
chr10:24377662..24388415hg19UCSC Ensembl
chr10:24417668..24428421hg18UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3810754
hg1910754
hg1810754
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1045300, nsv1047751
Samples
Known GenesKIAA1217
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv692n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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