A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3640032



Internal ID7026810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:14374475..14375362hg38UCSC Ensembl
Innerchr17:14374504..14375334hg38UCSC Ensembl
Outerchr17:14374447..14375391hg38UCSC Ensembl
chr17:14277792..14278679hg19UCSC Ensembl
Innerchr17:14277821..14278651hg19UCSC Ensembl
Outerchr17:14277764..14278708hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg38888
hg19888
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15621598, essv15621599, essv15621600
SamplesHG03999, HG03697, HG03890
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3640032
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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