A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614382



Internal ID6654588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:103756519..103758762hg38UCSC Ensembl
Innerchr7:103756519..103758762hg38UCSC Ensembl
Outerchr7:103756305..103758966hg38UCSC Ensembl
chr7:103396966..103399209hg19UCSC Ensembl
Innerchr7:103396966..103399209hg19UCSC Ensembl
Outerchr7:103396752..103399413hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg382244
hg192244
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12913143
SamplesHG02882
Known GenesRELN
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614382
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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