A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641256



Internal ID6681341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:75076931..75083469hg38UCSC Ensembl
Innerchr17:75076931..75083469hg38UCSC Ensembl
Outerchr17:75076431..75083969hg38UCSC Ensembl
chr17:73073026..73079564hg19UCSC Ensembl
Innerchr17:73073026..73079564hg19UCSC Ensembl
Outerchr17:73072526..73080064hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg386539
hg196539
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15740510, essv15740508, essv15740509
SamplesNA19399, NA19355, NA19308
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641256
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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