A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1607083



Internal ID12770203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:101728733..101728733hg38UCSC Ensembl
chr10:103488490..103488490hg19UCSC Ensembl
chr10:103478480..103478480hg18UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg38561
hg19561
hg18561
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3757365
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1607083
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