A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604794



Internal ID16045517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:142001319..142086604hg38UCSC Ensembl
Innerchr6:142322456..142407741hg19UCSC Ensembl
Innerchr6:142364149..142449434hg18UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg3885286
hg1985286
hg1885286
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1155788
SamplesHGDP01380
Known GenesNMBR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604794
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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