A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7612n100



Internal ID22793699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:61554104..61668092hg38UCSC Ensembl
chr9:44761942..44875930hg19UCSC Ensembl
chr9:44701938..44815926hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38113989
hg19113989
hg18113989
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1027743, nsv1023857, nsv1031128
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7612n100
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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