A curated catalogue of human genomic structural variation




Variant Details

Variant: esv34715



Internal ID12644065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:59096134..59179302hg38UCSC Ensembl
Innerchr10:60855894..60939062hg19UCSC Ensembl
Innerchr10:60525900..60609068hg18UCSC Ensembl
Innerchr10:60525900..60609068hg17UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3883169
hg1983169
hg1883169
hg1783169
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6978500, essv6986636, essv6978501, essv6978499
SamplesNA19127
Known GenesPHYHIPL
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)esv34715
Frequency
Sample Size771
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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