A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6477n100



Internal ID20158093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:76479432..76673974hg38UCSC Ensembl
chr7:76108749..76303291hg19UCSC Ensembl
chr7:75946685..76141227hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38194543
hg19194543
hg18194543
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1033529, nsv1022815, nsv1020909, nsv1033914
Samples
Known GenesDTX2, 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)dgv6477n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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