A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1074582



Internal ID15581082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:152069377..152071039hg38UCSC Ensembl
Innerchr6:152390512..152392174hg19UCSC Ensembl
Innerchr6:152432205..152433867hg18UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg381663
hg191663
hg181663
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv604906
Supporting Variants
Samples
Known GenesESR1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1074582
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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