A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604138



Internal ID16391547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:92064060..92114249hg38UCSC Ensembl
Innerchr6:92773778..92823967hg19UCSC Ensembl
Innerchr6:92830499..92880688hg18UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3850190
hg1950190
hg1850190
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1154182
SamplesHGDP00543
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604138
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