A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4265574



Internal ID11548112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:2377745..2378251hg38UCSC Ensembl
chr7:2417380..2417886hg19UCSC Ensembl
chr7:2383906..2384412hg18UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg38507
hg19507
hg18507
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1406872
Supporting Variants
SamplesHuRef
Known GenesEIF3B
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4265574
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