A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604563



Internal ID16391972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:120046039..120091997hg38UCSC Ensembl
Innerchr6:120367185..120413143hg19UCSC Ensembl
Innerchr6:120408884..120454842hg18UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3845959
hg1945959
hg1845959
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1154878
SamplesNINDS_125
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604563
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