A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6984994



Internal ID12983855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:37236694..37444453hg38UCSC Ensembl
Innerchr10:37525622..37733381hg19UCSC Ensembl
Innerchr10:37565628..37773387hg18UCSC Ensembl
Innerchr10:37565628..37773387hg17UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg38207760
hg19207760
hg18207760
hg17207760
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2750892
Supporting Variants
SamplesSPC_3
Known GenesLINC00993
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6984994
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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