A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021392



Internal ID19110609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:158192880..158252359hg38UCSC Ensembl
Innerchr7:157985572..158045051hg19UCSC Ensembl
Innerchr7:157678333..157737812hg18UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3859480
hg1959480
hg1859480
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3674736
Samples
Known GenesPTPRN2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1021392
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer