A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv930366



Internal ID15877636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:202033414..202035402hg38UCSC Ensembl
Innerchr2:202898137..202900125hg19UCSC Ensembl
Innerchr2:202606382..202608370hg18UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg381989
hg191989
hg181989
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv584172
Supporting Variants
Samples
Known GenesFZD7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv930366
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