A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13010747



Internal ID3012563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:150856424..150878664hg38UCSC Ensembl
chr7:150553512..150575752hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3822241
hg1922241
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3615471
Supporting Variants
SamplesNA19664
Known GenesAOC1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13010747
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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