A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3765636



Internal ID18966927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:8073011..8078395hg38UCSC Ensembl
chr19:8137895..8143279hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg385385
hg195385
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1072856
Supporting Variants
SamplesKWP1
Known GenesFBN3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3765636
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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