A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604908



Internal ID16045631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:152069414..152071039hg38UCSC Ensembl
Innerchr6:152390549..152392174hg19UCSC Ensembl
Innerchr6:152432242..152433867hg18UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg381626
hg191626
hg181626
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10973n54
Supporting Variantsnssv1074586, nssv1074588, nssv1074587
Samples
Known GenesESR1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604908
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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