A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641279



Internal ID7028053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:76257721..76264494hg38UCSC Ensembl
Innerchr17:76257721..76264494hg38UCSC Ensembl
Outerchr17:76257444..76264648hg38UCSC Ensembl
chr17:74253802..74260575hg19UCSC Ensembl
Innerchr17:74253802..74260575hg19UCSC Ensembl
Outerchr17:74253525..74260729hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg386774
hg196774
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15742596, essv15742597, essv15742595
SamplesHG03079, HG02546, HG02676
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641279
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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