A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1076284



Internal ID18979805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:24832188..24835020hg38UCSC Ensembl
chr1:25158679..25161511hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg382833
hg192833
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3769872
SamplesKWP1
Known GenesCLIC4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1076284
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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