A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv954035



Internal ID16956222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:38722258..38731557hg38UCSC Ensembl
Outerchr20:37350901..37360200hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg389300
hg199300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999974
SamplesBILGI_BIOE
Known GenesSLC32A1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv954035
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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