A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6480n100



Internal ID19016848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:76524019..76674181hg38UCSC Ensembl
chr7:76153336..76303498hg19UCSC Ensembl
chr7:75991272..76141434hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38150163
hg19150163
hg18150163
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1026894, nsv1032495
Samples
Known GenesLOC100133091, 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)dgv6480n100
Frequency
Sample Size29084
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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