A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604894



Internal ID16045617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:152068937..152070356hg38UCSC Ensembl
Innerchr6:152390072..152391491hg19UCSC Ensembl
Innerchr6:152431765..152433184hg18UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg381420
hg191420
hg181420
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10971n54
Supporting Variantsnssv1074469, nssv1074468
Samples
Known GenesESR1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604894
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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