A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3625659



Internal ID11789523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:436272..436272hg38UCSC Ensembl
chr5:436387..436387hg19UCSC Ensembl
chr5:489387..489387hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3875
hg1975
hg1875
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1017920
Supporting Variants
SamplesHuRef
Known GenesAHRR
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3625659
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