A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3690188



Internal ID18988469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:39445501..39878557hg38UCSC Ensembl
Innerchr9:41475094..42023575hg19UCSC Ensembl
Innerchr9:41465094..42013575hg18UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg38433057
hg19548482
hg18548482
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1034224
Supporting Variants
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)nssv3690188
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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