A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3772935



Internal ID18961515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:21513561..21515762hg38UCSC Ensembl
chr20:21494199..21496400hg19UCSC Ensembl
Cytoband20p11.22
Allele length
AssemblyAllele length
hg382202
hg192202
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1072108
Supporting Variants
SamplesKWP1
Known GenesNKX2-2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3772935
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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