A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3695252



Internal ID18646847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:129608081..129997996hg38UCSC Ensembl
Innerchr9:132370360..132760275hg19UCSC Ensembl
Innerchr9:131410181..131800096hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38389916
hg19389916
hg18389916
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1046477
Supporting Variants
Samples
Known GenesASB6, C9orf50, C9orf78, FNBP1, MIR6855, NTMT1, PRRX2, PTGES, TOR1A, TOR1B, USP20
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3695252
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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