A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6460n100



Internal ID20158076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:72532208..72889144hg38UCSC Ensembl
chr7:71997193..72359683hg19UCSC Ensembl
chr7:71635129..71997619hg18UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg38356937
hg19362491
hg18362491
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1031875, nsv1015994, nsv1030747, nsv1016734, nsv1026868, nsv1034054, nsv1027228
Samples
Known GenesMIR4650-1, MIR4650-2, POM121, SBDSP1, SPDYE7P, TYW1B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6460n100
Frequency
Sample Size29084
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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