A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1083556



Internal ID15936742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:44955728..44961619hg38UCSC Ensembl
Innerchr7:44995327..45001218hg19UCSC Ensembl
Innerchr7:44961852..44967743hg18UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg385892
hg195892
hg185892
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv606807
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)nssv1083556
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