A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7547n100



Internal ID22793634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:39455352..39878557hg38UCSC Ensembl
chr9:41600370..42023575hg19UCSC Ensembl
chr9:41590370..42013575hg18UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg38423206
hg19423206
hg18423206
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1022230, nsv1017869
Samples
Known GenesKGFLP2, LOC643648, LOC653501, MGC21881
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7547n100
Frequency
Sample Size11257
Observed Gain4
Observed Loss3
Observed Complex0
Frequencyn/a


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