A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6768n100



Internal ID22792855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:157200451..157231344hg38UCSC Ensembl
chr7:156993145..157024038hg19UCSC Ensembl
chr7:156685906..156716799hg18UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3830894
hg1930894
hg1830894
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1018281, nsv1019852
Samples
Known GenesUBE3C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6768n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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