A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7604n100



Internal ID19017972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:61520009..61993735hg38UCSC Ensembl
chr9:44727847..45129887hg19UCSC Ensembl
chr9:44667843..45069883hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38473727
hg19402041
hg18402041
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1018455, nsv1028842, nsv1032273
Samples
Known GenesFAM27C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7604n100
Frequency
Sample Size29084
Observed Gain26
Observed Loss0
Observed Complex0
Frequencyn/a


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