A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3640122



Internal ID7026899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:17088681..17099263hg38UCSC Ensembl
Innerchr17:17088719..17099226hg38UCSC Ensembl
Outerchr17:17088644..17099301hg38UCSC Ensembl
chr17:16991995..17002577hg19UCSC Ensembl
Innerchr17:16992033..17002540hg19UCSC Ensembl
Outerchr17:16991958..17002615hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3810583
hg1910583
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15633744
SamplesHG03449
Known GenesMPRIP
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3640122
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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