A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3615227



Internal ID7002116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:140321857..140376743hg38UCSC Ensembl
Innerchr7:140322007..140376593hg38UCSC Ensembl
Outerchr7:140321707..140376893hg38UCSC Ensembl
chr7:140021657..140076543hg19UCSC Ensembl
Innerchr7:140021807..140076393hg19UCSC Ensembl
Outerchr7:140021507..140076693hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3854887
hg1954887
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12983082
SamplesNA19663
Known GenesSLC37A3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3615227
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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