A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5161280



Internal ID7905994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:90180785..90787801hg38UCSC Ensembl
Innerchr10:91940542..92547558hg19UCSC Ensembl
Innerchr10:91930522..92537538hg18UCSC Ensembl
Innerchr10:91930522..92537538hg17UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg38607017
hg19607017
hg18607017
hg17607017
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2422237
Supporting Variants
SamplesND01566
Known GenesHTR7
MethodSNP array
Analysislog R ratio and B allele frequency.
PlatformNot specified
Comments
ReferenceSimon-Sanchez_et_al_2007
Pubmed ID17116639
Accession Number(s)essv5161280
Frequency
Sample Size181
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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