A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6366n100



Internal ID22792453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:56727783..57053295hg38UCSC Ensembl
chr7:56795476..57121002hg19UCSC Ensembl
chr7:56762970..57124944hg18UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg38325513
hg19325527
hg18361975
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1016071, nsv1019894, nsv1021343, nsv1017155
Samples
Known GenesLOC100130849, MIR4283-1, MIR4283-2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6366n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss18
Observed Complex0
Frequencyn/a


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