A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3697569



Internal ID18995850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:95486046..95496896hg38UCSC Ensembl
Innerchr9:98248328..98259178hg19UCSC Ensembl
Innerchr9:97288149..97298999hg18UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg3810851
hg1910851
hg1810851
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1053434
Supporting Variants
Samples
Known GenesPTCH1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3697569
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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