A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1257856



Internal ID12420979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:136074463..136074463hg38UCSC Ensembl
chr9:138966309..138966309hg19UCSC Ensembl
chr9:138106130..138106130hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38480
hg19480
hg18480
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4242928
SamplesHuRef
Known GenesNACC2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1257856
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