A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641320



Internal ID7028094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:77925457..77927570hg38UCSC Ensembl
Innerchr17:77925607..77927420hg38UCSC Ensembl
Outerchr17:77925307..77927720hg38UCSC Ensembl
chr17:75921539..75923652hg19UCSC Ensembl
Innerchr17:75921689..75923502hg19UCSC Ensembl
Outerchr17:75921389..75923802hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg382114
hg192114
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15748500, essv15748502, essv15748503, essv15748501
SamplesHG02690, HG03685, HG03805, HG02682
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641320
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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