A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6978501



Internal ID12635398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:59106134..59136534hg38UCSC Ensembl
Innerchr10:60865894..60896294hg19UCSC Ensembl
Innerchr10:60535900..60566300hg18UCSC Ensembl
Innerchr10:60535900..60566300hg17UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3830401
hg1930401
hg1830401
hg1730401
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34715
Supporting Variants
SamplesNA19127
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6978501
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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