A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3690197



Internal ID18641792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:39445501..40228945hg38UCSC Ensembl
Innerchr9:41475094..42373963hg19UCSC Ensembl
Innerchr9:41465094..42363959hg18UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg38783445
hg19898870
hg18898866
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1020579
Supporting Variants
Samples
Known GenesANKRD20A2, ANKRD20A3, KGFLP2, LOC643648, LOC653501, MGC21881, SPATA31A5, SPATA31A7, ZNF658B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3690197
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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