A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6276n100



Internal ID22792363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:12503535..12580115hg38UCSC Ensembl
chr7:12543161..12619740hg19UCSC Ensembl
chr7:12509686..12586265hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3876581
hg1976580
hg1876580
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1027831, nsv1025397
Samples
Known GenesSCIN
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6276n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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