A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051665



Internal ID19140884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:95472122..95502295hg38UCSC Ensembl
Innerchr9:98234404..98264577hg19UCSC Ensembl
Innerchr9:97274225..97304398hg18UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg3830174
hg1930174
hg1830174
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3697568
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)nsv1051665
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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