A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6598n100



Internal ID22792685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:119652709..119966749hg38UCSC Ensembl
chr7:119292763..119606803hg19UCSC Ensembl
chr7:119079999..119394039hg18UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg38314041
hg19314041
hg18314041
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1024175, nsv1029023, nsv1023813, nsv1029841
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)dgv6598n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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