A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3640316



Internal ID7027091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:28869243..28877137hg38UCSC Ensembl
Innerchr17:28869319..28877061hg38UCSC Ensembl
Outerchr17:28869167..28877213hg38UCSC Ensembl
chr17:27196261..27204155hg19UCSC Ensembl
Innerchr17:27196337..27204079hg19UCSC Ensembl
Outerchr17:27196185..27204231hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg387895
hg197895
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15656948
SamplesHG00421
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3640316
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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