A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639921



Internal ID7026699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:9754224..9757409hg38UCSC Ensembl
Innerchr17:9754224..9757409hg38UCSC Ensembl
Outerchr17:9753955..9757623hg38UCSC Ensembl
chr17:9657541..9660726hg19UCSC Ensembl
Innerchr17:9657541..9660726hg19UCSC Ensembl
Outerchr17:9657272..9660940hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg383186
hg193186
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15610357
SamplesNA19452
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639921
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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