A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4220309



Internal ID11156161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1592380..1592380hg38UCSC Ensembl
chr10:1634575..1634575hg19UCSC Ensembl
chr10:1624575..1624575hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3864
hg1964
hg1864
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1278410
Supporting Variants
SamplesHuRef
Known GenesADARB2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4220309
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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