A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6990881



Internal ID10371650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:65176750..65697209hg38UCSC Ensembl
Innerchr7:64637128..65162182hg19UCSC Ensembl
Innerchr7:64274563..64799617hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38520460
hg19525055
hg18525055
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2764020
Supporting Variants
SamplesSW_1413
Known GenesINTS4L2, LOC441242, ZNF92
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)essv6990881
Frequency
Sample Size1109
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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