A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6983865



Internal ID12630626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:3134171..3164173hg38UCSC Ensembl
Innerchr10:3176363..3206365hg19UCSC Ensembl
Innerchr10:3166363..3196365hg18UCSC Ensembl
Innerchr10:3166363..3196365hg17UCSC Ensembl
Cytoband10p15.2
Allele length
AssemblyAllele length
hg3830003
hg1930003
hg1830003
hg1730003
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2750891
Supporting Variants
SamplesBEC_727
Known GenesPFKP, PITRM1, PITRM1-AS1
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6983865
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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