A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7541n100



Internal ID22793628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:39445501..39833345hg38UCSC Ensembl
chr9:41475094..41978363hg19UCSC Ensembl
chr9:41465094..41968363hg18UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg38387845
hg19503270
hg18503270
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1023869, nsv1018682, nsv1026994
Samples
Known GenesKGFLP2, 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)dgv7541n100
Frequency
Sample Size11257
Observed Gain28
Observed Loss3
Observed Complex0
Frequencyn/a


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