A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3640009



Internal ID7026787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:13998297..14002832hg38UCSC Ensembl
Innerchr17:13998297..14002832hg38UCSC Ensembl
Outerchr17:13997797..14003332hg38UCSC Ensembl
chr17:13901614..13906149hg19UCSC Ensembl
Innerchr17:13901614..13906149hg19UCSC Ensembl
Outerchr17:13901114..13906649hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg384536
hg194536
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15617993
SamplesNA19189
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3640009
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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