A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3612294



Internal ID6999195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:13413888..13418402hg38UCSC Ensembl
Innerchr7:13413888..13418402hg38UCSC Ensembl
Outerchr7:13413685..13418616hg38UCSC Ensembl
chr7:13453513..13458027hg19UCSC Ensembl
Innerchr7:13453513..13458027hg19UCSC Ensembl
Outerchr7:13453310..13458241hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg384515
hg194515
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12684940, essv12684939, essv12684941
SamplesNA20866, HG04159, HG04153
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3612294
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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