A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3769849



Internal ID18966425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:47785255..47785856hg38UCSC Ensembl
chr20:46413999..46414600hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg38602
hg19602
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1073065
Supporting Variants
SamplesKWP1
Known GenesSULF2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3769849
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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