A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3768897



Internal ID19307149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:16139752..16139812hg38UCSC Ensembl
chr8:15997261..15997321hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1075117
Supporting Variants
SamplesKWP1
Known GenesMSR1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3768897
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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