A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6435644



Internal ID8882899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:65127104..65133103hg38UCSC Ensembl
Outerchr17:65126947..65133256hg38UCSC Ensembl
Innerchr17:63123222..63129221hg19UCSC Ensembl
Outerchr17:63123065..63129374hg19UCSC Ensembl
Cytoband17q24.1
Allele length
AssemblyAllele length
hg386310
hg196310
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2658428
Supporting Variants
SamplesHG00334
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6435644
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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