A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4331197



Internal ID11613735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:82752734..82752734hg38UCSC Ensembl
chr13:83326869..83326869hg19UCSC Ensembl
chr13:82224870..82224870hg18UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3850
hg1950
hg1850
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1643312
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4331197
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