A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6978500



Internal ID12635397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:59106096..59136505hg38UCSC Ensembl
Innerchr10:60865856..60896265hg19UCSC Ensembl
Innerchr10:60535862..60566271hg18UCSC Ensembl
Innerchr10:60535862..60566271hg17UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3830410
hg1930410
hg1830410
hg1730410
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)essv6978500
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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