A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3564878



Internal ID6689574
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 OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv989075
Supporting Variants
SamplesHuRef
Known GenesESR1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3564878
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