A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6982569



Internal ID12628529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46188858..46313658hg38UCSC Ensembl
Innerchr10:47560094..47684894hg19UCSC Ensembl
Innerchr10:47030100..47154900hg18UCSC Ensembl
Innerchr10:47030100..47154900hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38124801
hg19124801
hg18124801
hg17124801
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2750958
Supporting Variants
SamplesBEC_568
Known GenesANTXRL, ANTXRLP1
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6982569
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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