A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614287



Internal ID6654494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99967058..99969085hg38UCSC Ensembl
Innerchr7:99967065..99969079hg38UCSC Ensembl
Outerchr7:99967052..99969092hg38UCSC Ensembl
chr7:99564681..99566708hg19UCSC Ensembl
Innerchr7:99564688..99566702hg19UCSC Ensembl
Outerchr7:99564675..99566715hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg382028
hg192028
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12908901, essv12908900
SamplesNA18952, NA18984
Known GenesAZGP1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614287
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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