A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604911



Internal ID16392320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:152070046..152071426hg38UCSC Ensembl
Innerchr6:152391181..152392561hg19UCSC Ensembl
Innerchr6:152432874..152434254hg18UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg381381
hg191381
hg181381
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10974n54
Supporting Variantsnssv1074594, nssv1074595, nssv1074593, nssv1074592
Samples
Known GenesESR1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604911
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer