A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6983864



Internal ID12630629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:3121393..3160490hg38UCSC Ensembl
Innerchr10:3163585..3202682hg19UCSC Ensembl
Innerchr10:3153585..3192682hg18UCSC Ensembl
Innerchr10:3153585..3192682hg17UCSC Ensembl
Cytoband10p15.2
Allele length
AssemblyAllele length
hg3839098
hg1939098
hg1839098
hg1739098
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 Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6983864
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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