A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3612945



Internal ID6999844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:41398651..41403488hg38UCSC Ensembl
Innerchr7:41398684..41403455hg38UCSC Ensembl
Outerchr7:41398618..41403521hg38UCSC Ensembl
chr7:41438249..41443086hg19UCSC Ensembl
Innerchr7:41438282..41443053hg19UCSC Ensembl
Outerchr7:41438216..41443119hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg384838
hg194838
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12752175
SamplesNA18984
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3612945
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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