A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3615197



Internal ID7002086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:138678044..138691465hg38UCSC Ensembl
Innerchr7:138678044..138691465hg38UCSC Ensembl
Outerchr7:138677544..138691965hg38UCSC Ensembl
chr7:138362789..138376210hg19UCSC Ensembl
Innerchr7:138362789..138376210hg19UCSC Ensembl
Outerchr7:138362289..138376710hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3813422
hg1913422
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12981553, essv12981551, essv12981552
SamplesHG01843, HG00590, HG01870
Known GenesSVOPL
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3615197
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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