A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3772789



Internal ID19310333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:85750249..85869780hg38UCSC Ensembl
chr8:86762478..86882009hg19UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg38119532
hg19119532
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1075153
Supporting Variants
SamplesKWP1
Known GenesREXO1L1, REXO1L2P
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3772789
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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