A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639624



Internal ID7026403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:370897..446617hg38UCSC Ensembl
chr17:220688..296408hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg3875721
hg1975721
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15571332
SamplesHG01935
Known GenesC17orf97, FAM101B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639624
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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