A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3640047



Internal ID7026825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:14781492..15004377hg38UCSC Ensembl
Innerchr17:14781492..15004377hg38UCSC Ensembl
Outerchr17:14780992..15004877hg38UCSC Ensembl
chr17:14684809..14907694hg19UCSC Ensembl
Innerchr17:14684809..14907694hg19UCSC Ensembl
Outerchr17:14684309..14908194hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg38222886
hg19222886
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15623428
SamplesHG03572
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3640047
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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