A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10971n54



Internal ID20144395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:152068937..152070356hg38UCSC Ensembl
chr6:152390072..152391491hg19UCSC Ensembl
chr6:152431765..152433184hg18UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg381420
hg191420
hg181420
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv604894, nsv604893
Samples
Known GenesESR1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10971n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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