A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6378n100



Internal ID22792465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:57638217..57960277hg38UCSC Ensembl
chr7:57697923..58019983hg19UCSC Ensembl
chr7:57701865..58023925hg18UCSC Ensembl
Cytoband7p11.1
Allele length
AssemblyAllele length
hg38322061
hg19322061
hg18322061
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1025576, nsv1023594
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)dgv6378n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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