A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10973n54



Internal ID20144397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:152069271..152071039hg38UCSC Ensembl
chr6:152390406..152392174hg19UCSC Ensembl
chr6:152432099..152433867hg18UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg381769
hg191769
hg181769
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv604908, nsv604905, nsv604909, nsv604906, nsv604907, nsv604903
Samples
Known GenesESR1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10973n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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