A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641224



Internal ID7027998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:73693607..73698287hg38UCSC Ensembl
Innerchr17:73693607..73698287hg38UCSC Ensembl
Outerchr17:73693437..73698448hg38UCSC Ensembl
chr17:71689746..71694426hg19UCSC Ensembl
Innerchr17:71689746..71694426hg19UCSC Ensembl
Outerchr17:71689576..71694587hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg384681
hg194681
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15737253, essv15737254
SamplesHG02887, HG02837
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641224
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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