A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1485241



Internal ID12301677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:150372580..150372644hg38UCSC Ensembl
chr6:150693716..150693780hg19UCSC Ensembl
chr6:150735409..150735473hg18UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3865
hg1965
hg1865
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4337701
SamplesHuRef
Known GenesIYD
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1485241
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