A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3613962



Internal ID7000857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:84287237..84306398hg38UCSC Ensembl
Innerchr7:84287278..84306357hg38UCSC Ensembl
Outerchr7:84287196..84306439hg38UCSC Ensembl
chr7:83916553..83935714hg19UCSC Ensembl
Innerchr7:83916594..83935673hg19UCSC Ensembl
Outerchr7:83916512..83935755hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3819162
hg1919162
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1307e214
Supporting Variantsessv12875151, essv12875150, essv12875152
SamplesNA19397, HG02977, HG04054
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3613962
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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