A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614410



Internal ID7001304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:104928207..104930597hg38UCSC Ensembl
Innerchr7:104928231..104930574hg38UCSC Ensembl
Outerchr7:104928184..104930621hg38UCSC Ensembl
chr7:104568654..104571044hg19UCSC Ensembl
Innerchr7:104568678..104571021hg19UCSC Ensembl
Outerchr7:104568631..104571068hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg382391
hg192391
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12913415, essv12913416, essv12913417
SamplesHG02952, HG02317, NA19711
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614410
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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