A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6318n100



Internal ID22792405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:32169581..32392762hg38UCSC Ensembl
chr7:32209193..32432374hg19UCSC Ensembl
chr7:32175718..32398899hg18UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg38223182
hg19223182
hg18223182
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1033812, nsv1016345, nsv1020972, nsv1019139, nsv1033713, nsv1028414, nsv1025986
Samples
Known GenesPDE1C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6318n100
Frequency
Sample Size11257
Observed Gain11
Observed Loss0
Observed Complex0
Frequencyn/a


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