A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6986246



Internal ID12628752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46188877..46290653hg38UCSC Ensembl
Innerchr10:47560113..47661889hg19UCSC Ensembl
Innerchr10:47030119..47131895hg18UCSC Ensembl
Innerchr10:47030119..47131895hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38101777
hg19101777
hg18101777
hg17101777
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2750960
Supporting Variants
SamplesBEC_581
Known GenesANTXRL, ANTXRLP1
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6986246
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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