A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6722n100



Internal ID22792809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:143776585..143878995hg38UCSC Ensembl
chr7:143473678..143576088hg19UCSC Ensembl
chr7:143104611..143207021hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38102411
hg19102411
hg18102411
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1024463, nsv1029770, nsv1025690, nsv1022022, nsv1024119, nsv1031131, nsv1032640
Samples
Known GenesFAM115A, LOC154761
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6722n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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