A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3615225



Internal ID7002114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:140304131..140310244hg38UCSC Ensembl
Innerchr7:140304131..140310244hg38UCSC Ensembl
Outerchr7:140303961..140310378hg38UCSC Ensembl
chr7:140003931..140010044hg19UCSC Ensembl
Innerchr7:140003931..140010044hg19UCSC Ensembl
Outerchr7:140003761..140010178hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg386114
hg196114
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12983078, essv12983075, essv12983073, essv12983077, essv12983076, essv12983080, essv12983079, essv12983074
SamplesNA18597, NA18560, HG02409, NA18537, HG00479, NA20851, NA18615, NA18609
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3615225
Frequency
Sample Size2504
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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