A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036609



Internal ID19125828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:93612935..93715359hg38UCSC Ensembl
Innerchr9:96375217..96477641hg19UCSC Ensembl
Innerchr9:95415038..95517462hg18UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38102425
hg19102425
hg18102425
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3697558
Samples
Known GenesPHF2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036609
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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