A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3615471



Internal ID6655670
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13010744, essv13010746, essv13010745, essv13010747, essv13010743
SamplesNA19664, NA12762, HG02104, HG01092, HG01086
Known GenesAOC1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3615471
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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