A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639974



Internal ID7026752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:12594688..12597496hg38UCSC Ensembl
Innerchr17:12594703..12597482hg38UCSC Ensembl
Outerchr17:12594674..12597511hg38UCSC Ensembl
chr17:12498005..12500813hg19UCSC Ensembl
Innerchr17:12498020..12500799hg19UCSC Ensembl
Outerchr17:12497991..12500828hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg382809
hg192809
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15612985, essv15612987, essv15612986
SamplesNA19072, NA18994, HG03077
Known GenesLINC00670
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639974
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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