A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3640739



Internal ID6680825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:49302051..49303596hg38UCSC Ensembl
Innerchr17:49302076..49303572hg38UCSC Ensembl
Outerchr17:49302027..49303621hg38UCSC Ensembl
chr17:47379413..47380958hg19UCSC Ensembl
Innerchr17:47379438..47380934hg19UCSC Ensembl
Outerchr17:47379389..47380983hg19UCSC Ensembl
Cytoband17q21.32
Allele length
AssemblyAllele length
hg381546
hg191546
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15694641
SamplesHG02143
Known GenesZNF652
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3640739
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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