A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3615687



Internal ID7002576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:157287928..157289101hg38UCSC Ensembl
Innerchr7:157287978..157288948hg38UCSC Ensembl
Outerchr7:157287878..157289151hg38UCSC Ensembl
chr7:157080622..157081795hg19UCSC Ensembl
Innerchr7:157080672..157081642hg19UCSC Ensembl
Outerchr7:157080572..157081845hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg381174
hg191174
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13040089, essv13040090, essv13040091, essv13040093, essv13040088, essv13040087, essv13040092
SamplesHG02339, HG02888, HG02703, HG03556, NA19317, NA19026, HG03557
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3615687
Frequency
Sample Size2504
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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