A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3640057



Internal ID7026835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:15106320..15108731hg38UCSC Ensembl
Innerchr17:15106320..15108731hg38UCSC Ensembl
Outerchr17:15106104..15108972hg38UCSC Ensembl
chr17:15009637..15012048hg19UCSC Ensembl
Innerchr17:15009637..15012048hg19UCSC Ensembl
Outerchr17:15009421..15012289hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg382412
hg192412
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15623566
SamplesHG04222
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3640057
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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