A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639656



Internal ID7026434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:918873..936966hg38UCSC Ensembl
chr17:822113..840206hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg3818094
hg1918094
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15578154
SamplesHG00629
Known GenesNXN
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639656
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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