A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7601n100



Internal ID22793688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:61520009..61629677hg38UCSC Ensembl
chr9:44727847..44837515hg19UCSC Ensembl
chr9:44667843..44777511hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38109669
hg19109669
hg18109669
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1027504, nsv1020620, nsv1030799, nsv1030789, nsv1017937
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)dgv7601n100
Frequency
Sample Size11257
Observed Gain345
Observed Loss738
Observed Complex0
Frequencyn/a


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