A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6470n100



Internal ID19016838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:76443262..76671318hg38UCSC Ensembl
chr7:76072579..76300635hg19UCSC Ensembl
chr7:75910515..76138571hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38228057
hg19228057
hg18228057
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1031785, nsv1021715
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)dgv6470n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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