A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3640991



Internal ID7027765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:63397702..63398559hg38UCSC Ensembl
Innerchr17:63397752..63398509hg38UCSC Ensembl
Outerchr17:63397626..63398635hg38UCSC Ensembl
chr17:61475063..61475920hg19UCSC Ensembl
Innerchr17:61475113..61475870hg19UCSC Ensembl
Outerchr17:61474987..61475996hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg38858
hg19858
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15720741
SamplesHG01565
Known GenesTANC2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3640991
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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