A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3640431



Internal ID7027206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:34788849..34795228hg38UCSC Ensembl
Innerchr17:34788862..34795215hg38UCSC Ensembl
Outerchr17:34788836..34795241hg38UCSC Ensembl
chr17:33115868..33122247hg19UCSC Ensembl
Innerchr17:33115881..33122234hg19UCSC Ensembl
Outerchr17:33115855..33122260hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg386380
hg196380
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15664058, essv15664056, essv15664057
SamplesNA20507, NA19720, HG02223
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3640431
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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