A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3612958



Internal ID6999857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:42360424..42364812hg38UCSC Ensembl
Innerchr7:42360448..42364788hg38UCSC Ensembl
Outerchr7:42360400..42364836hg38UCSC Ensembl
chr7:42400023..42404411hg19UCSC Ensembl
Innerchr7:42400047..42404387hg19UCSC Ensembl
Outerchr7:42399999..42404435hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg384389
hg194389
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12752246
SamplesHG00128
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3612958
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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