A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611558



Internal ID6651776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:162589023..162674622hg38UCSC Ensembl
chr6:163010055..163095654hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3885600
hg1985600
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1237e214
Supporting Variantsessv12621516
SamplesHG01620
Known GenesPARK2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611558
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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