A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6765n100



Internal ID22792852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155191409..155229504hg38UCSC Ensembl
chr7:154983119..155021214hg19UCSC Ensembl
chr7:154614052..154652147hg18UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg3838096
hg1938096
hg1838096
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1022929, nsv1020492, nsv1017881
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6765n100
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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