A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6535n100



Internal ID22792622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:97756249..97775599hg38UCSC Ensembl
chr7:97385561..97404911hg19UCSC Ensembl
chr7:97223497..97242847hg18UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3819351
hg1919351
hg1819351
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1025219, nsv1025306, nsv1021820
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)dgv6535n100
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer