A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3615028



Internal ID7001917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:130841097..130848775hg38UCSC Ensembl
Innerchr7:130841103..130848770hg38UCSC Ensembl
Outerchr7:130841092..130848781hg38UCSC Ensembl
chr7:130525856..130533534hg19UCSC Ensembl
Innerchr7:130525862..130533529hg19UCSC Ensembl
Outerchr7:130525851..130533540hg19UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg387679
hg197679
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12972052, essv12972051
SamplesHG02078, HG02140
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3615028
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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