A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639685



Internal ID7026463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:1430039..1436256hg38UCSC Ensembl
Innerchr17:1430054..1436241hg38UCSC Ensembl
Outerchr17:1430024..1436271hg38UCSC Ensembl
chr17:1333333..1339550hg19UCSC Ensembl
Innerchr17:1333348..1339535hg19UCSC Ensembl
Outerchr17:1333318..1339565hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg386218
hg196218
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15580895
SamplesHG02970
Known GenesCRK
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639685
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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