A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1076858



Internal ID18971079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:150743523..150744524hg38UCSC Ensembl
chr1:150715999..150717000hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg381002
hg191002
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3770744
SamplesKWP1
Known GenesCTSS
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1076858
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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