A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6985502



Internal ID12626240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46432359..46606223hg38UCSC Ensembl
Innerchr10:46943394..47117394hg19UCSC Ensembl
Innerchr10:46363400..46537400hg18UCSC Ensembl
Innerchr10:46363400..46537400hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38173865
hg19174001
hg18174001
hg17174001
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2750902
Supporting Variants
SamplesBEC_361
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)essv6985502
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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