A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6370n100



Internal ID22792457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:57220433..57960277hg38UCSC Ensembl
chr7:57288140..58019983hg19UCSC Ensembl
chr7:57292082..58023925hg18UCSC Ensembl
Cytoband7p11.1
Allele length
AssemblyAllele length
hg38739845
hg19731844
hg18731844
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1019359, nsv1030441
Samples
Known GenesMIR3147, ZNF716
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6370n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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