A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027875



Internal ID19117093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:158074929..158310123hg38UCSC Ensembl
Innerchr7:157867621..158102815hg19UCSC Ensembl
Innerchr7:157560382..157795576hg18UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38235195
hg19235195
hg18235195
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3674734
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)nsv1027875
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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