A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2750888



Internal ID12984440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:26936718..26952851hg38UCSC Ensembl
Innerchr10:27225647..27241780hg19UCSC Ensembl
Innerchr10:27265653..27281786hg18UCSC Ensembl
Innerchr10:27265653..27281786hg17UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3816134
hg1916134
hg1816134
hg1716134
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6987681, essv6988848
SamplesSPC_18
Known GenesLINC00202-1
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Affymetrix Mapping 250K Sty2 SNP Array
CommentsSample level SV from stringent call set
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)esv2750888
Frequency
Sample Size771
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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