A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6982570



Internal ID12628528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46188877..46370859hg38UCSC Ensembl
Innerchr10:47560113..47742076hg19UCSC Ensembl
Innerchr10:47030119..47212082hg18UCSC Ensembl
Innerchr10:47030119..47212082hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38181983
hg19181964
hg18181964
hg17181964
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2750958
Supporting Variants
SamplesBEC_568
Known GenesANTXRL, ANTXRLP1, FAM25B
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6982570
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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