A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3772916



Internal ID18964701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:2715935..2716000hg38UCSC Ensembl
chr20:2696581..2696646hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1072097
Supporting Variants
SamplesKWP1
Known GenesEBF4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3772916
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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