A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4192655



Internal ID11128507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1409658..1410103hg38UCSC Ensembl
chr10:1451853..1452298hg19UCSC Ensembl
chr10:1441853..1442298hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38446
hg19446
hg18446
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1543111
Supporting Variants
SamplesHuRef
Known GenesADARB2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4192655
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