A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv603162



Internal ID16043885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:55292014..55361215hg38UCSC Ensembl
Innerchr6:55156812..55226013hg19UCSC Ensembl
Innerchr6:55264771..55333972hg18UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg3869202
hg1969202
hg1869202
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1060839
Samples
Known GenesGFRAL
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv603162
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