A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6522n100



Internal ID22792609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:85934047..86130557hg38UCSC Ensembl
chr7:85563363..85759873hg19UCSC Ensembl
chr7:85401299..85597809hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38196511
hg19196511
hg18196511
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1017226, nsv1028233
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)dgv6522n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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