A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3610701



Internal ID12151167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:98393019..98393181hg38UCSC Ensembl
chr7:98022331..98022493hg19UCSC Ensembl
chr7:97860267..97860429hg18UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg38163
hg19163
hg18163
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1113502
Supporting Variants
SamplesHuRef
Known GenesBAIAP2L1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3610701
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