A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3612639



Internal ID6999539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:26551103..26566959hg38UCSC Ensembl
chr7:26590722..26606578hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg3815857
hg1915857
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1276e214
Supporting Variantsessv12710789, essv12710790, essv12710788
SamplesHG03905, NA19309, NA19439
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3612639
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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