A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12682884



Internal ID745305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:10616036..10747477hg38UCSC Ensembl
Innerchr7:10616036..10747477hg38UCSC Ensembl
Outerchr7:10615536..10747977hg38UCSC Ensembl
chr7:10655663..10787104hg19UCSC Ensembl
Innerchr7:10655663..10787104hg19UCSC Ensembl
Outerchr7:10655163..10787604hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38131442
hg19131442
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3612193
Supporting Variants
SamplesHG00351
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12682884
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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