A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3757741



Internal ID19056022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:158210950..158300141hg38UCSC Ensembl
Innerchr7:158003642..158092833hg19UCSC Ensembl
Innerchr7:157696403..157785594hg18UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3889192
hg1989192
hg1889192
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1034867
Supporting Variants
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)nssv3757741
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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