A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029216



Internal ID19118435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:39445501..39990996hg38UCSC Ensembl
Innerchr9:41475094..42136014hg19UCSC Ensembl
Innerchr9:41465094..42126014hg18UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg38545496
hg19660921
hg18660921
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7542n100
Supporting Variantsnssv3690195, nssv3690196, nssv3690194
Samples
Known GenesKGFLP2, 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)nsv1029216
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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