A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2764049



Internal ID10378085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:97756261..97777749hg38UCSC Ensembl
Innerchr7:97385573..97407061hg19UCSC Ensembl
Innerchr7:97223509..97244997hg18UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3821489
hg1921489
hg1821489
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv151e203
Supporting Variantsessv6990980, essv6990985, essv6990981, essv6990987, essv6990984, essv6990971, essv6990982, essv6990970, essv6990974, essv6990962, essv6990965, essv6990978, essv6990976, essv6990973, essv6990964, essv6990977, essv6990963, essv6990969, essv6990972, essv6990983, essv6990975, essv6990986, essv6990966
SamplesSW_1372, SW_1021, SW_0030, SW_0620, SW_0099, SW_0816, SW_1106, SW_0200, SW_1055, SW_0062, SW_1243, SW_1196, SW_1506, SW_0663, SW_1265, SW_1018, SW_0524, SW_1180, SW_1424, SW_1046, SW_1267, SW_1303, SW_1250
Known Genes
MethodMerging
AnalysisTwo different algorithms (PennCNV and Birdseye) were applied to detect CNVs. Only congruent CNV events regarding direction of effect that were detected by both algorithms were merged using the outer borders of the event in a first step. In a second step only CNVs that were detected in at least two individuals were merged into a CNVR.
PlatformMerging
Comments
ReferenceVogler_et_al_2010
Pubmed ID21179565
Accession Number(s)esv2764049
Frequency
Sample Size1109
Observed Gain6
Observed Loss17
Observed Complex0
Frequencyn/a


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