A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15578159



Internal ID1770676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:939223..948350hg38UCSC Ensembl
chr17:842463..851590hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg389128
hg199128
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3639659
Supporting Variants
SamplesHG01628
Known GenesNXN
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15578159
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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