A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604903



Internal ID16045626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:152069271..152071039hg38UCSC Ensembl
Innerchr6:152390406..152392174hg19UCSC Ensembl
Innerchr6:152432099..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 Variantsdgv10973n54
Supporting Variantsnssv1074579
Samples
Known GenesESR1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604903
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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