A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3640451



Internal ID6680538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:35482860..35501389hg38UCSC Ensembl
Innerchr17:35482906..35501343hg38UCSC Ensembl
Outerchr17:35482814..35501435hg38UCSC Ensembl
chr17:33809879..33828408hg19UCSC Ensembl
Innerchr17:33809925..33828362hg19UCSC Ensembl
Outerchr17:33809833..33828454hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3818530
hg1918530
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15664525
SamplesHG02385
Known GenesSLFN12L
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3640451
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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