A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3769192



Internal ID18961175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:158659518..158659908hg38UCSC Ensembl
chr1:158629308..158629698hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg38391
hg19391
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1077748
Supporting Variants
SamplesKWP1
Known GenesSPTA1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3769192
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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