A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6596n100



Internal ID22792683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:119203154..119391719hg38UCSC Ensembl
chr7:118843208..119031773hg19UCSC Ensembl
chr7:118630444..118819009hg18UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg38188566
hg19188566
hg18188566
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1027982, nsv1019838
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)dgv6596n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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