A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1009406



Internal ID6721509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1118089..1118260hg38UCSC Ensembl
chr10:1164029..1164200hg19UCSC Ensembl
chr10:1154029..1154200hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38172
hg19172
hg18172
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3572728
SamplesHuRef
Known GenesWDR37
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1009406
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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