A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952691



Internal ID17301565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:22273538..22274237hg38UCSC Ensembl
Outerchr18:19853501..19854200hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38700
hg19700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998856
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952691
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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