A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1091195



Internal ID15944381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:95391290..95395591hg38UCSC Ensembl
Innerchr7:95020602..95024903hg19UCSC Ensembl
Innerchr7:94858538..94862839hg18UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg384302
hg194302
hg184302
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv607862
Supporting Variants
Samples
Known GenesPON3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1091195
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