A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3597804



Internal ID6984942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:131741501..131782608hg38UCSC Ensembl
chr3:131460345..131501452hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg3841108
hg1941108
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv937e214
Supporting Variantsessv11151999, essv11152000
SamplesHG01047, NA19467
Known GenesCPNE4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3597804
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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