A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10970n54



Internal ID20144394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:152068833..152071039hg38UCSC Ensembl
chr6:152389968..152392174hg19UCSC Ensembl
chr6:152431661..152433867hg18UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg382207
hg192207
hg182207
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv604898, nsv604895, nsv604902, nsv604896, nsv604897, nsv604891, nsv604899, nsv604892, nsv604901
Samples
Known GenesESR1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10970n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss106
Observed Complex0
Frequencyn/a


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