A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519010



Internal ID15099617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:151979492..151987997hg38UCSC Ensembl
Innerchr6:152300627..152309132hg19UCSC Ensembl
Innerchr6:152342320..152350825hg18UCSC Ensembl
Innerchr6:152392741..152401246hg17UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg388506
hg198506
hg188506
hg178506
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696479
Samples
Known GenesESR1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519010
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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