A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641390



Internal ID7028164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:81004030..81020768hg38UCSC Ensembl
Innerchr17:81004043..81020756hg38UCSC Ensembl
Outerchr17:81004018..81020781hg38UCSC Ensembl
chr17:78977830..78994568hg19UCSC Ensembl
Innerchr17:78977843..78994556hg19UCSC Ensembl
Outerchr17:78977818..78994581hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3816739
hg1916739
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15760177, essv15760179, essv15760178, essv15760176, essv15760175, essv15760180
SamplesHG02360, HG02407, HG00458, HG00531, HG00476, HG02182
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641390
Frequency
Sample Size2504
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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