A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6984993



Internal ID12983854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:37236694..37352620hg38UCSC Ensembl
Innerchr10:37525622..37641548hg19UCSC Ensembl
Innerchr10:37565628..37681554hg18UCSC Ensembl
Innerchr10:37565628..37681554hg17UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg38115927
hg19115927
hg18115927
hg17115927
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)essv6984993
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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