A curated catalogue of human genomic structural variation




Variant Details

Variant: esv34440



Internal ID12643793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46412752..46572051hg38UCSC Ensembl
Innerchr10:46977566..47136996hg19UCSC Ensembl
Innerchr10:46397572..46557002hg18UCSC Ensembl
Innerchr10:46397572..46557002hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38159300
hg19159431
hg18159431
hg17159431
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv22e55
Supporting Variantsessv6988570, essv6982693
SamplesBEC_580
Known GenesGPRIN2, HNRNPA1P33, LINC00842, LOC100996758, NPY4R
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
CommentsSample level SV from stringent call set
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)esv34440
Frequency
Sample Size771
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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