A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024913



Internal ID19114130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:158323687..158382204hg38UCSC Ensembl
Innerchr7:158116379..158174896hg19UCSC Ensembl
Innerchr7:157809140..157867657hg18UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3858518
hg1958518
hg1858518
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6770n100
Supporting Variantsnssv3674739
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)nsv1024913
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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