A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891171



Internal ID18838881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:102577953..102682009hg38UCSC Ensembl
Outerchr7:102577953..102693659hg38UCSC Ensembl
Innerchr7:102218400..102322456hg19UCSC Ensembl
Outerchr7:102218400..102334106hg19UCSC Ensembl
Innerchr7:102005497..102109692hg18UCSC Ensembl
Outerchr7:102005497..102121342hg18UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38115707
hg19115707
hg18115846
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25787292, essv25781374
Samples
Known GenesPOLR2J2, POLR2J3, RASA4, RASA4B, SPDYE2, SPDYE2B, UPK3BL
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891171
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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