A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6512n100



Internal ID22792599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:79687161..79780757hg38UCSC Ensembl
chr7:79316477..79410073hg19UCSC Ensembl
chr7:79154413..79248009hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3893597
hg1993597
hg1893597
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1025266, nsv1020043, nsv1016075, nsv1023653, nsv1033114, nsv1018854
Samples
Known GenesMIR548M
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6512n100
Frequency
Sample Size11257
Observed Gain16
Observed Loss0
Observed Complex0
Frequencyn/a


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