A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4202625



Internal ID11138477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:12518474..12520988hg38UCSC Ensembl
chr10:12560473..12562987hg19UCSC Ensembl
chr10:12600479..12602993hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg382515
hg192515
hg182515
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1750238
Supporting Variants
SamplesHuRef
Known GenesCAMK1D
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4202625
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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