A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3612631



Internal ID6652844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:26185776..26187351hg38UCSC Ensembl
Innerchr7:26185797..26187330hg38UCSC Ensembl
Outerchr7:26185755..26187372hg38UCSC Ensembl
chr7:26225396..26226971hg19UCSC Ensembl
Innerchr7:26225417..26226950hg19UCSC Ensembl
Outerchr7:26225375..26226992hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg381576
hg191576
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12710508
SamplesHG02373
Known GenesNFE2L3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3612631
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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