A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604904



Internal ID16045627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:152069271..152071426hg38UCSC Ensembl
Innerchr6:152390406..152392561hg19UCSC Ensembl
Innerchr6:152432099..152434254hg18UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg382156
hg192156
hg182156
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10972n54
Supporting Variantsnssv1074580
Samples
Known GenesESR1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604904
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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