A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3640030



Internal ID7026808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:14352963..14355111hg38UCSC Ensembl
Innerchr17:14352978..14355097hg38UCSC Ensembl
Outerchr17:14352949..14355126hg38UCSC Ensembl
chr17:14256280..14258428hg19UCSC Ensembl
Innerchr17:14256295..14258414hg19UCSC Ensembl
Outerchr17:14256266..14258443hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg382149
hg192149
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15621595
SamplesHG04156
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3640030
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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