A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035073



Internal ID19124292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:158074929..158231024hg38UCSC Ensembl
Innerchr7:157867621..158023716hg19UCSC Ensembl
Innerchr7:157560382..157716477hg18UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38156096
hg19156096
hg18156096
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3674733
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)nsv1035073
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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