A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6345n100



Internal ID20157961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:47668927..47791937hg38UCSC Ensembl
chr7:47708525..47831535hg19UCSC Ensembl
chr7:47675050..47798060hg18UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg38123011
hg19123011
hg18123011
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1018608, nsv1022906
Samples
Known GenesLINC00525, PKD1L1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6345n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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