A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2422253



Internal ID7906350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:27142437..27286441hg38UCSC Ensembl
Innerchr10:27431366..27575370hg19UCSC Ensembl
Innerchr10:27471372..27615376hg18UCSC Ensembl
Innerchr10:27471372..27615376hg17UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38144005
hg19144005
hg18144005
hg17144005
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5161310
SamplesND01701
Known GenesACBD5, LRRC37A6P, MASTL, YME1L1
MethodSNP array
Analysislog R ratio and B allele frequency.
PlatformNot specified
Comments
ReferenceSimon-Sanchez_et_al_2007
Pubmed ID17116639
Accession Number(s)esv2422253
Frequency
Sample Size181
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer