A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15674161



Internal ID5500680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:38926876..38928813hg38UCSC Ensembl
Innerchr17:38926876..38928813hg38UCSC Ensembl
Outerchr17:38926703..38928999hg38UCSC Ensembl
chr17:37083129..37085066hg19UCSC Ensembl
Innerchr17:37083129..37085066hg19UCSC Ensembl
Outerchr17:37082956..37085252hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg381938
hg191938
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3640532
Supporting Variants
SamplesNA18985
Known GenesLINC00672
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15674161
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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