A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3766072



Internal ID11649113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:87111003..87111335hg38UCSC Ensembl
chr4:88032155..88032487hg19UCSC Ensembl
chr4:88251179..88251511hg18UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg38333
hg19333
hg18333
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1030392
Supporting Variants
SamplesHuRef
Known GenesAFF1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3766072
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