A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6354n100



Internal ID22792441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:54117556..54129851hg38UCSC Ensembl
chr7:54185249..54197544hg19UCSC Ensembl
chr7:54152743..54165038hg18UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg3812296
hg1912296
hg1812296
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1027409, nsv1030559, nsv1030703, nsv1018998
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)dgv6354n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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