A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1074139



Internal ID15927325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:143548325..143550439hg38UCSC Ensembl
Innerchr6:143869462..143871576hg19UCSC Ensembl
Innerchr6:143911155..143913269hg18UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg382115
hg192115
hg182115
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv604797
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1074139
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