A curated catalogue of human genomic structural variation




Variant Details

Variant: esv989075



Internal ID6725045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:152068650..152071574hg38UCSC Ensembl
Outerchr6:152389785..152392709hg19UCSC Ensembl
Outerchr6:152431478..152434402hg18UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg382925
hg192925
hg182925
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3564878
SamplesHuRef
Known GenesESR1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv989075
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer