A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6986995



Internal ID12981129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46432404..46606240hg38UCSC Ensembl
Innerchr10:46943377..47117349hg19UCSC Ensembl
Innerchr10:46363383..46537355hg18UCSC Ensembl
Innerchr10:46363383..46537355hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38173837
hg19173973
hg18173973
hg17173973
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34875
Supporting Variants
SamplesNA18940
Known GenesGPRIN2, LINC00842, LOC100996758, NPY4R, SYT15
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6986995
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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