A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13993631



Internal ID3995447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:2983355..3019578hg38UCSC Ensembl
chr11:3004585..3040808hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3836224
hg1936224
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625132
Supporting Variants
SamplesHG00154
Known GenesCARS, NAP1L4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13993631
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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