A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12738486



Internal ID2740302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:37200495..37213762hg38UCSC Ensembl
chr7:37240100..37253367hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3813268
hg1913268
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3612846
Supporting Variants
SamplesHG02763
Known GenesELMO1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12738486
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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