A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641019



Internal ID7027793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:63915506..63921390hg38UCSC Ensembl
chr17:61992866..61998750hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg385885
hg195885
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15722769, essv15722771, essv15722770
SamplesNA19057, HG00622, NA12749
Known GenesGH1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641019
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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