A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13689281



Internal ID6232847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:7038300..7084697hg38UCSC Ensembl
chr10:7080262..7126659hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3846398
hg1946398
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622264
Supporting Variants
SamplesNA19758
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13689281
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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