A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6472n100



Internal ID19016840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:76443262..76803016hg38UCSC Ensembl
chr7:76072579..76432333hg19UCSC Ensembl
chr7:75910515..76270269hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38359755
hg19359755
hg18359755
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1033715, nsv1020370
Samples
Known GenesDTX2, FDPSP2, LOC100133091, POMZP3, UPK3B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6472n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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