A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6979049



Internal ID12632869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:75801755..75940477hg38UCSC Ensembl
Innerchr10:77561513..77700235hg19UCSC Ensembl
Innerchr10:77231519..77370241hg18UCSC Ensembl
Innerchr10:77231519..77370241hg17UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38138723
hg19138723
hg18138723
hg17138723
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34687
Supporting Variants
SamplesNA12872
Known GenesC10orf11
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6979049
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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