A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3612627



Internal ID6652840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:26174292..26175322hg38UCSC Ensembl
Innerchr7:26174332..26175282hg38UCSC Ensembl
Outerchr7:26174252..26175362hg38UCSC Ensembl
chr7:26213912..26214942hg19UCSC Ensembl
Innerchr7:26213952..26214902hg19UCSC Ensembl
Outerchr7:26213872..26214982hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg381031
hg191031
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12710379
SamplesNA19090
Known GenesNFE2L3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3612627
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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