A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604907



Internal ID16045630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:152069414..152070924hg38UCSC Ensembl
Innerchr6:152390549..152392059hg19UCSC Ensembl
Innerchr6:152432242..152433752hg18UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg381511
hg191511
hg181511
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10973n54
Supporting Variantsnssv1074585
Samples
Known GenesESR1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604907
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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