A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1082929



Internal ID11899368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1396818..1396900hg38UCSC Ensembl
chr10:1439013..1439095hg19UCSC Ensembl
chr10:1429013..1429095hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3883
hg1983
hg1883
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4330089
SamplesHuRef
Known GenesADARB2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1082929
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