A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6528n100



Internal ID22792615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:89696294..89927701hg38UCSC Ensembl
chr7:89325608..89557015hg19UCSC Ensembl
chr7:89163544..89394951hg18UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg38231408
hg19231408
hg18231408
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1033642, nsv1023682
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)dgv6528n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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