A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv609212



Internal ID16396621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:157552088..157558005hg38UCSC Ensembl
Innerchr7:157344782..157350699hg19UCSC Ensembl
Innerchr7:157037543..157043460hg18UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg385918
hg195918
hg185918
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1100521
Samples
Known GenesPTPRN2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv609212
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