A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1048713



Internal ID15901899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:4255153..4472353hg38UCSC Ensembl
Innerchr6:4255387..4472587hg19UCSC Ensembl
Innerchr6:4200386..4417586hg18UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg38217201
hg19217201
hg18217201
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv600863
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)nssv1048713
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