A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12819204



Internal ID1050234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:66465188..66476943hg38UCSC Ensembl
Innerchr7:66465208..66476924hg38UCSC Ensembl
Outerchr7:66465169..66476963hg38UCSC Ensembl
chr7:65930175..65941930hg19UCSC Ensembl
Innerchr7:65930195..65941911hg19UCSC Ensembl
Outerchr7:65930156..65941950hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg3811756
hg1911756
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3613508
Supporting Variants
SamplesHG00672
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12819204
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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